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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 92373

123 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
May 25, 2023
Product types
Device
Classifications
Class I
Statuses
Ongoing
Recalling firm wording
TELEFLEX LLC

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

123 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 123

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170050

Z-1827-2023
Recall number
Z-1827-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
11560 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI: 4026704319534, Batch numbers: 18FG05, 18GG08, 18GT32, 18HG38, 18JG02, 18JG11, 18KG15, 18LG22, 19AG24, 19DT06, 19DT33, 19ET28, 19FT18, 19IT25, 19KT48, 20AT14, 20DT09, 20ET04, 20GT31, KME20J1235, KME20J1238, KME20K2551, KME20L1089, KME20L2371, KME21A2064, KME21B2498, KME21F1552, KME21G1708, KME21K1248, KME21M2648, KME22B1391, KME22D1768, KME22D1769

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 2 of 123

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170055

Z-1828-2023
Recall number
Z-1828-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
3530 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 4026704319541, Batch numbers: 18FG18, 18GG14, 18GG31, 18HG22, 18KG23, 19BG12, 19ET72, 19IT25, 20AT25, 20AT32, 20BT05, 20BT37, 20BT47, 20ET21, KME20G0383, KME20K0936, KME20K2587, KME20L1469, KME20L2378, KME21G0756, KME21M0313, KME21M1832, KME22B0193, KME22D1787, KME22F1665

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 3 of 123

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170060

Z-1829-2023
Recall number
Z-1829-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
9400 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 4026704319558, Batch numbers: 18GG31, 18HG22, 18HG32, 18HG35, 18IG09, 18IG24, 18IG27, 18JG17, 18LG12, 19AG37, 19BG12, 19CT49, 19DT15, 19DT20, 19ET22, 19ET38, 19ET77, 19FT18, 19IT14, 19IT25, 19JT42, 20DT29, 20ET04, 20FT34, 20FT54, 20GG41, KME20H1653, KME20J1236, KME20J1237, KME20L1487, KME20L2379, KME20M0494, KME21A0384, KME21A1482, KME21C0293, KME21E1411, KME21G0757, KME21G2208, KME21G2209, KME21K0548, KME21K0549, KME21L0444, KME21M1392, KME22A1512, KME22A1513, KME22B1392

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 4 of 123

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170065

Z-1830-2023
Recall number
Z-1830-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
15020

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/ID 4026704319565, Batch numbers: 18FG05, 18FG25, 18GG05, 18GG10, 18GG20, 18GT32, 18HG19, 18HG32, 18HG38, 18IG09, 18JG04, 18JG06, 18JG34, 18KG35, 19AG13, 19AG37, 19BG01, 19CT58, 19CT71, 19DT15, 19ET60, 19FT41, 19GT38, 19HT15, 19HT61, 19HT66, 19IT25, 19JT18, 19JT22, 19JT57, 19JT70, 19KT41, 20AT25, 20AT53, 20BT27, 20CT05, 20CT22, 20DT37, 20ET21, 20GT14, KME20H0903, KME20H0904, KME20H2018, KME20J1239, KME20J1240, KME20K0938, KME20K2623, KME20L0487, KME20L1705, KME20M1578, KME20M1751, KME21K1127, KME21K1256, KME21K3029

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 5 of 123

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170070

Z-1831-2023
Recall number
Z-1831-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
50039 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 4026704319572, Batch numbers: 18FG09, 18FG15, 18FG17, 18FG20, 18FG21, 18GG10, 18GG28, 18GT32, 18HG07, 18HG16, 18HG35, 18HG38, 18IG09, 18JG02, 18JG17, 18JG37, 18KG23, 18KG35, 18LG05, 18LG12, 18LG18, 19AG13, 19AG31, 19AG34, 19BG04, 19CT17, 19CT41, 19CT49, 19CT55, 19FT24, 19FT41, 19GT05, 19GT10, 19GT52, 19GT59, 19GT65, 19HT40, 19HT66, 19IT44, 19IT54, 19JT22, 19JT42, 19JT57, 19JT64, 19KT30, 19KT41, 19LT04, 19LT17, 20AT14, 20AT25, 20AT44, 20AT53, 20BT05, 20BT23, 20BT47, 20CT05, 20CT12, 20CT27, 20CT51, 20DT09, 20DT37, 20ET16, 20ET56, 20FT10, 20FT54, 20GG36, 20GG45, KME20H0245, KME20H1287, KME20H1288, KME20J0571, KME20J0572, KME20J0802, KME20J3033, KME20K2544, KME20L0053, KME20L0055, KME20L0942, KME20L2372, KME20M0381, KME20M1103, KME20M1755, KME21A0893, KME21B1074, KME21B1075, KME21D1430, KME21E1290, KME21F1526, KME21G0541, KME21G0542, KME21G0543, KME21G1559, KME21H0608, KME21K0551, KME21K1767, KME21K2469, KME21L1897

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 6 of 123

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170075

Z-1832-2023
Recall number
Z-1832-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
38950 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 4026704319589, Batch numbers: 18FG09, 18FG15, 18FG17, 18FG22, 18FG30, 18FT32, 18GG02, 18GG05, 18GG28, 18GT32, 18HG12, 18HG16, 18HG22, 18HG27, 18HG38, 18IG06, 18IG15, 18IG17, 18IG27, 18JG02, 18JG11, 18JG26, 18KG07, 18KG18, 18KG44, 18LG12, 18LG22, 19AG13, 19AG27, 19AG34, 19AG37, 19BG07, 19CT41, 19CT49, 19CT55, 19FT14, 19FT18, 19FT35, 19GT10, 19GT52, 19GT59, 19GT65, 19HT10, 19HT35, 19HT48, 19IT06, 19IT14, 19IT25, 19IT44, 19JT22, 19JT49, 19JT70, 19KT25, 19LT04, 19LT32, 20AT14, 20AT25, 20AT32, 20AT44, 20AT53, 20BG12, 20BT47, 20CT36, 20CT51, 20DT09, 20DT37, 20ET16, 20ET37, 20FT54, 20FT61, KME20H0977, KME20H0979, KME20J0575, KME20J2715, KME20K1352, KME20L1132, KME20M0033, KME20M0382, KME20M1149, KME20M1225, KME20M1227, KME20M1537, KME20M2881, KME20M2882, KME21A0824, KME21D1785, KME21F1326, KME21F1327, KME21G0544, KME21K1410, KME21L2179, KME21L2346, KME21L2347, KME21M0195, KME21M0869, KME21M0965, KME21M1267

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 7 of 123

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170080

Z-1833-2023
Recall number
Z-1833-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
18150 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 4026704319596, Batch Numbers: 18FG09, 18FG20, 18FT32, 18GG05, 18GG08, 18GG14, 18HG07, 18HG12, 18HG22, 18HG27, 18HG35, 18IG02, 18IG09, 18IG15, 18JG04, 18JG06, 18JG14, 18JG26, 18LG12, 18LG18, 19AG13, 19AG24, 19AG27, 19AG31, 19BG01, 19CT41, 19DT38, 19ET38, 19ET45, 19ET50, 19FT24, 19GT59, 19IT06, 19IT25, 19IT54, 19JT42, 19JT49, 19JT57, 19KT25, 19LT04, 20AT14, 20AT25, 20AT32, 20AT37, 20AT53, 20BT05, 20BT47, 20CT05, 20CT12, 20CT27, 20CT36, 20CT51, 20DT09, 20FT44, 20GT25, KME20H0248, KME20H2019, KME20L0396, KME20L1278, KME20L1279, KME20L2830, KME20M0847, KME21A0386, KME21A2800, KME21A2801, KME21B1245, KME21B2156, KME21C0533, KME21D1204, KME21E1287, KME21F1329, KME21J0410, KME21L0274, KME21L0813, KME21L0851, KME22E2351

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 8 of 123

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170085

Z-1834-2023
Recall number
Z-1834-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
4370 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 4026704319602, Batch Numbers: 18FG09, 18GG20, 18GG28, 18HG07, 18JG11, 18KG18, 19AG37, 19CT32, 19DT02, 19ET38, 19ET60, 19HT61, 19HT66, 19IT44, 19KT21, 19KT55, 19LT32, 20AT32, 20BT05, 20BT23, 20CT51, 20GG36, KME20L0398, KME20L2376, KME20M3247, KME21C0298, KME21E1296, KME21K1876, KME21L0573, KME22F0484

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 9 of 123

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170090

Z-1835-2023
Recall number
Z-1835-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
1460 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 4026704319619, Batch Numbers: 18FG09, 18HG27, 18IG12, 18LG18, 19GT52, 19GT65, 19HT35, 20AT25, KME20L0625, KME21E1232, KME22E2491, KME22E2912

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 10 of 123

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170095

Z-1836-2023
Recall number
Z-1836-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
720 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 4026704319626, Batch Numbers: 19HT48, 19KT17, 20AT53, 20BT37, KME22E2493, KME22F1387, KME22H0342

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 11 of 123

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170120

Z-1837-2023
Recall number
Z-1837-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
14160 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704644879, Batch Numbers: 18JG23, 18JG26, 18JG34, 18KG26, 18LG05, 19AG18, 19AG21, 19AG24, 19AG37, 19BG01, 19BG04, 19BG07, 19BG12, 19BG16, 19CT58, 19CT71, 19DT06, 19DT20, 19ET77, 19FT14, KME20H0975, KME20H0976, KME20J0324, KME20K0771, KME20K2545, KME20K2568, KME20L0627, KME21A1886, KME21B1671, KME21B2506, KME21C2475, KME21D0447, KME21K1723, KME22A0056, KME22B0179, KME22B0180, KME22B0181, KME22B0464, KME22C2255, KME22C2256, KME22D1638, KME22D1639, KME22D1788, KME22E1489, KME22F1500, KME22F1669, KME22F1670, KME22G3099, KME22H3107, KME22H3275, KME22J2354, KME22J2355, KME22J2356, KME23A2360

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 12 of 123

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170125

Z-1838-2023
Recall number
Z-1838-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
18900 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704644886, Batch Numbers: 18JG11, 18JG26, 18JG34, 18KG18, 18KG23, 18LG15, 18LG22, 19AG09, 19AG21, 19AG24, 19AG37, 19BG04, 19BG07, 19BG12, 19BG16, 19BG21, 19CT41, 19CT49, 19CT55, 19DT38, 19ET45, 19ET77, 19FT24, 19GT59, 19HT35, 20CT51, 20DT37, 20ET16, 20ET28, 20GG41, 20GG45, KME20J0332, KME20K0948, KME20K2546, KME20L0629, KME20L0630, KME20L0631, KME20L1484, KME20L2399, KME20M0810, KME21A1887, KME21A1888, KME21B0577, KME21B1142, KME21C0490, KME21C3427, KME21C3428, KME21D1022, KME21K1724, KME21K1725, KME21K1726, KME21L1891, KME21L1892, KME21M0433, KME21M1817, KME22B0724, KME22B0929, KME22B1072, KME22C0912, KME22D0786, KME22D3646, KME22D3647, KME22E1131, KME22E1237, KME22E2262, KME22F2865, KME22F2867, KME22G0565, KME22G1099, KME22G1517, KME22H1628, KME22H1899

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 13 of 123

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170130

Z-1839-2023
Recall number
Z-1839-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
22400 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704644893, Batch Numbers: 18JG09, 18JG26, 18JG34, 18JG37, 18KG18, 18KG23, 18LG02, 18LG22, 19AG09, 19AG21, 19AG37, 19BG04, 19BG07, 19BG21, 19BG40, 19CT49, 19CT71, 19DT33, 19ET22, 19ET28, 19ET54, 19ET60, 19ET72, 19ET77, 19FT24, 19GT59, 19GT65, 19HT35, 19HT66, 19IT25, 19JT22, 19JT29, 20AT53, 20BT23, 20BT27, 20BT47, 20CT12, 20CT36, 20CT51, 20DT09, 20DT37, 20ET16, 20ET28, 20GT06, KME20H2016, KME20J0326, KME20K0155, KME20K0156, KME20K1885, KME20K2582, KME20K3586, KME20L1485, KME20L1836, KME20L1837, KME20L2400, KME20M0812, KME21A1895, KME21A1896, KME21A2805, KME21A2806, KME21B0578, KME21B1677, KME21C0532, KME21C0534, KME21C2645, KME21C3512, KME21C3513, KME21D1023, KME21D1429, KME21J1143, KME21J1407, KME21J1408, KME21L2341, KME21L2342, KME21M0030, KME22B2145, KME22C0914, KME22C1231, KME22C1232, KME22C1823, KME22C2258, KME22C2260, KME22C3451, KME22E1030, KME22F0301, KME22G0908, KME22G0909, KME22H0667, KME22J0698, KME22K0017, KME22K0919, KME22K0920, KME22K3076

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 14 of 123

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170135

Z-1840-2023
Recall number
Z-1840-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
20662 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704647030, Batch Numbers: 18KG03, 18KG07, 18KG18, 18LG22, 19AG18, 19AG21, 19AG24, 19AG37, 19BG04, 19BG12, 19BG40, 19CT49, 19CT58, 19DT06, 19DT20, 19DT38, 19ET22, 19ET28, 19GT45, 19GT59, 19GT65, 19HT05, 19HT35, 19HT61, 19HT66, 19IT54, 19JT22, 19JT29, 20AT32, 20AT53, 20BT05, 20BT23, 20BT47, 20CT12, 20CT36, 20DT09, 20DT37, 20ET16, 20ET21, 20ET28, KME20G0242, KME20H1846, KME20J0328, KME20J1234, KME20K1629, KME20K2547, KME20K2583, KME20K3590, KME20L0632, KME20L1486, KME20L2401, KME20M0811, KME20M3276, KME20M3277, KME21A1898, KME21A2813, KME21B1686, KME21C0018, KME21D1850, KME21E0464, KME21K1250, KME21L1893, KME21L1894, KME21L2343, KME22A0207, KME22A1510, KME22B0538, KME22B0726, KME22B1029, KME22B2334, KME22C1825, KME22C2261, KME22E2104, KME22E2263, KME22E2264, KME22F2163, KME22F2418, KME22H0050, KME22H0350, KME22H2625, KME22J0996

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 15 of 123

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170140

Z-1841-2023
Recall number
Z-1841-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
10650 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704647047, Batch Numbers: 18JG17, 18JG32, 18JG34, 18KG29, 18LG02, 18LG15, 18LG18, 19AG09, 19AG21, 19BG12, 19CT32, 19DT06, 19DT20, 19ET38, 19ET72, 19ET77, 19FT24, 19JT29, 20BG16, 20CT36, 20DT37, 20ET28, 20GG45, 20GT14, KME20H2017, KME20K0772, KME20K2549, KME20K2584, KME20L1491, KME20L2402, KME21A1159, KME21A1900, KME21A2810, KME21B0572, KME21B1688, KME21C0024, KME21C0493, KME21C2999, KME21L1921, KME21L1922, KME22B1077, KME22C2262, KME22C3452, KME22E1239, KME22F0049, KME22F1951, KME22H0913, KME22H0967, KME22H2910

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 16 of 123

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170145

Z-1842-2023
Recall number
Z-1842-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
4320 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704644923, Batch Numbers: 18JG14, 18LG15, 19AG24, 19BG12, 19BG16, 19CT49, 19IT25, 20BT05, 20CT12, 20CT51, 20DT29, 20GG41, KME20H2929, KME20K1886, KME20K2586, KME20L1488, KME20L2377, KME21A1891, KME21C0019, KME21C1566, KME21C1974, KME21D0445, KME21J1149, KME21M1818, KME21M2952, KME22D1896, KME22E1744

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 17 of 123

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170150

Z-1843-2023
Recall number
Z-1843-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
2940 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704644930, Batch Numbers: 18JG21, 18KG18, 19AG09, 19AG37, 19CT32, 19DT33, 19ET38, 19ET77, 19GT45, 19IT54, 20DT29, 20ET56, KME20K0157, KME20L1845, KME20L1846, KME21A0892, KME21B1697, KME21J0153, KME22B1390, KME22B2161, KME22C3335, KME22C3453, KME22F1351, KME22F2419

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 18 of 123

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170155

Z-1844-2023
Recall number
Z-1844-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
3310 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704644947, Batch Numbers: 18JG17, 19AG37, 19CT32, 19ET22, 19ET38, 19ET60, 19IT54, 20AT32, 20CT22, 20DT29, KME20G0385, KME20K2550, KME20L1492, KME20M0813, KME21A2775, KME21B1698, KME21C2646, KME21J0882, KME21J0883, KME22F0239, KME22F0718, KME22F2420, KME22J0254, KME22J0262, KME22K2780

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 19 of 123

Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504550

Z-1845-2023
Recall number
Z-1845-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
66310 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 4026704547579, Batch Numbers: 18FG03, 18FG13, 18GG12, 18GG17, 18GG31, 18HG12, 18IG02, 18IG12, 18IG21, 18IG27, 18JG02, 18KG15, 18LG25, 18LG37, 19AG37, 19BG07, 19BG21, 19CT71, 19ET54, 19FT14, 19FT24, 19GT10, 19GT20, 19GT38, 19GT65, 19HT05, 19HT40, 19HT66, 19JT70, 19KT08, 19LT17, 19LT32, 20AT14, 20AT25, 20BT27, 20BT37, 20CT36, 20CT54, 20DT14, 20ET04, 20ET21, 20GT38, KME20H0128, KME20K0001, KME20K0467, KME20K1581, KME20L0618, KME20L1090, KME20L2027, KME20M0019, KME21D1964, KME21F1551, KME21G1707, KME21K0545, KME21K1249, KME21M0011, KME21M1831, KME21M2074, KME21M2647, KME22B0171, KME22B0172, KME22B1395, KME22B1632, KME22C0436, KME22C1654, KME22C3003, KME22D0145, KME22D0825, KME22E1129, KME22H0163, KME22H1169, KME22H1703, KME22H1709, KME22J3162, KME22J3163

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 20 of 123

Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504555

Z-1846-2023
Recall number
Z-1846-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
42214 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 4026704547586, Batch Numbers: 18FG20, 18FG22, 18FG25, 18FT32, 18GG14, 18HG12, 18HG27, 18IG06, 18IG24, 18IG27, 18JG02, 18JG14, 18KG07, 18KG23, 18KG35, 18LG31, 19AG27, 19BG04, 19CT55, 19ET72, 19FT30, 19GT05, 19GT10, 19GT20, 19GT38, 19GT59, 19GT65, 19HT61, 19IT25, 19JT29, 19JT42, 19JT49, 19KT30, 19KT41, 19LT04, 19LT50, 20AT09, 20AT44, 20BT05, 20BT13, 20BT27, 20BT37, 20CT05, 20CT12, 20CT36, 20ET21, KME20G0388, KME20J0319, KME20J2321, KME21H1189, KME22A0148, KME22A2939, KME22A2940, KME22A3267, KME22A3268, KME22B1633, KME22B1751, KME22C3207, KME22D0590, KME22D1785, KME22E0619, KME22E0620, KME22F1666, KME22G0225, KME22G2294, KME22H3105, KME22J1458, KME22J1459, KME22J2714, KME22L1104, KME22L1105, KME23C0590

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 21 of 123

Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504560

Z-1847-2023
Recall number
Z-1847-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
103842 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 4026704547593, Batch Numbers: 18FG03, 18FG15, 18FG28, 18GG24, 18IG27, 18JG02, 18JG17, 18JG26, 18JG34, 18KG09, 18KG35, 18LG05, 18LG12, 18LG18, 18LG37, 19AG27, 19AG37, 19BG12, 19CT32, 19CT41, 19CT55, 19CT58, 19ET66, 19ET77, 19FT14, 19FT24, 19FT35, 19GT05, 19GT45, 19HT05, 19HT61, 19JT42, 19KT17, 19KT21, 19KT65, 19LT04, 19LT23, 20AT09, 20AT37, 20AT53, 20BT51, 20CT05, 20CT12, 20CT36, 20DT37, 20ET04, 20FT10, 20FT35, 20GT06, KME20H0129, KME20H0906, KME20H1791, KME20H1847, KME20J0848, KME20K1550, KME20L0336, KME20M0492, KME21E1412, KME21G2207, KME21H0839, KME21H0972, KME21H1124, KME21K0660, KME21K1165, KME21L0442, KME21L0443, KME21L1900, KME21L2539, KME21M1391, KME22A1432, KME22B1411, KME22C1068, KME22C2858, KME22D0479, KME22D0482, KME22D0592, KME22D2846

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 22 of 123

Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504565

Z-1848-2023
Recall number
Z-1848-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
92930 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 4026704547609, Batch Numbers: 18FG05, 18FG13, 18FG25, 18GG20, 18HG07, 18HG12, 18HG19, 18HG32, 18HG38, 18IG06, 18IG09, 18IG15, 18JG04, 18JG21, 18JG34, 18KG35, 18LG39, 19AG01, 19AG24, 19AG27, 19AG37, 19CT32, 19CT41, 19CT58, 19CT65, 19DT06, 19DT20, 19DT33, 19ET32, 19ET54, 19ET60, 19FT24, 19FT41, 19GT28, 19GT38, 19HT10, 19HT66, 19IT14, 19IT25, 19JT18, 19JT29, 19JT42, 19JT57, 19KT08, 19KT41, 19KT55, 19LT32, 20AT09, 20AT14, 20AT25, 20AT53, 20BT27, 20CT05, 20CT12, 20CT36, 20CT44, 20DT09, 20ET04, 20ET16, 20GT14, KME20G0189, KME20G0316, KME20H2312, KME20H2585, KME20H2586, KME20H2587, KME20J0320, KME20J0570, KME20K0465, KME20K0939, KME20K1551, KME20K1628, KME20K2246, KME20L0488, KME20L1840, KME20M0022, KME20M0854, KME20M1102, KME20M1579, KME21K1128, KME21L0328, KME21L2340, KME21M2283, KME21M2446, KME21M2568, KME22A0675, KME22A2415, KME22A3028, KME22A3156, KME22A3313, KME22B0067, KME22B1218, KME22B1409, KME22C0499, KME22C0863, KME22C1073, KME22C1225, KME22C1655, KME22C1941, KME22D0747, KME22D0755, KME22F1616, KME22F1617, KME22G0632, KME22G1224, KME22G2467, KME22H1900, KME22H3348, KME22J1135, KME22J1136, KME22J1928, KME22J3352, KME22K2413, KME22K2414, KME22L0241, KME22L0242, KME22L1792

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 23 of 123

Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504570

Z-1849-2023
Recall number
Z-1849-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
1051810 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 4026704547616, Batch Numbers: 18FG03, 18FG13, 18FG21, 18FG22, 18FG30, 18FT32, 18GG02, 18GG08, 18GG20, 18GT32, 18HG07, 18HG16, 18HG19, 18HG32, 18HG35, 18HG38, 18IG02, 18IG06, 18IG12, 18IG17, 18IG24, 18IG27, 18JG02, 18JG04, 18JG21, 18JG32, 18JG37, 18KG23, 18KG35, 18KG38, 18LG05, 18LG08, 18LG12, 18LG18, 18LG31, 18LG39, 19AG05, 19AG09, 19AG31, 19AG34, 19BG04, 19CG06, 19CT17, 19CT23, 19CT32, 19CT37, 19CT49, 19CT55, 19CT58, 19CT65, 19CT71, 19DT25, 19DT33, 19DT45, 19ET05, 19ET15, 19ET22, 19ET28, 19ET45, 19ET60, 19FT14, 19FT24, 19FT30, 19FT41, 19GT05, 19GT10, 19GT20, 19GT59, 19GT65, 19HT40, 19HT53, 19IT25, 19IT32, 19IT39, 19IT44, 19IT54, 19JT22, 19JT57, 19JT64, 19JT70, 19KT17, 19KT25, 19KT48, 19KT55, 19LT04, 19LT10, 19LT32, 19LT38, 19LT50, 20AT09, 20AT14, 20AT25, 20AT32, 20AT44, 20AT53, 20AT57, 20BG12, 20BT05, 20BT23, 20BT27, 20BT37, 20BT47, 20CT05, 20CT12, 20CT22, 20CT27, 20CT36, 20CT44, 20DT14, 20DT37, 20ET04, 20ET16, 20FT10, 20FT39, 20FT54, 20FT61, 20GG45, 20GG47, 20GT06, 20GT25, 20GT31, 20GT38, KME20H0972, KME20H1935, KME20H2588, KME20H2783, KME20J0058, KME20J0060, KME20J0156, KME20J0321, KME20J0573, KME20J0574, KME20J0803, KME20J0804, KME20J0805, KME20J0946, KME20J1112, KME20J1233, KME20J1692, KME20J1694, KME20J2175, KME20J2577, KME20J2957, KME20J3035, KME20K0026, KME20K0360, KME20K0361, KME20K0768, KME20K0941, KME20K1148, KME20K1202, KME20K1304, KME20K1552, KME20K1658, KME20K2057, KME20K2187, KME20K3161, KME20K3355, KME20L0057, KME20L0059, KME20L0490, KME20L0623, KME20L0943, KME20L0944, KME20L1091, KME20L1122, KME20L1124, KME20L1475, KME20L1844, KME20L2039, KME20L2258, KME20L2827, KME20M0378, KME20M0379, KME20M0380, KME20M0498, KME21G0508, KME21G1162, KME21G1179, KME21G1354, KME21G1355, KME21G1379, KME21G1385, KME21G1705, KME21G1782, KME21G2060, KME21G2061, KME21G2090, KME21H0604, KME21H0605, KME21H0607, KME21H0776, KME21H0777, KME21J1183, KME21J1206, KME21J1244, KME21J1255, KME21J1258, KME21J1482, KME21J1604, KME21J1747, KME21J2053, KME21K0016, KME21K0261, KME21K0271, KME21K0272, KME21K0314, KME21K0554, KME21K0662, KME21K0728, KME21K0830, KME21K1041, KME21K1044, KME21K1331, KME21K1413, KME21K1503, KME21K1517, KME21K1556, KME21K1620, KME21K1845, KME21K2355, KME21K2356, KME21L0093, KME21L0094, KME21L0768, KME21L1053, KME21L1054, KME21L1216, KME21L1217, KME21L1277, KME21L1966, KME21L2129, KME21L2690, KME21L2811, KME21M1888, KME21M2117, KME21M2320, KME21M2562, KME21M2845, KME21M3200, KME22A0150, KME22A0245, KME22A0390, KME22A0698, KME22A0797, KME22A0798, KME22A0990, KME22A1135, KME22A1161, KME22A1257, KME22A3253, KME22A3254, KME22A3312, KME22B0301, KME22B0354, KME22B0522, KME22B0523, KME22B0536, KME22B0537, KME22B0624, KME22B0633, KME22B0684, KME22B0849, KME22B0943, KME22B0985, KME22B1396, KME22B1408, KME22B1472, KME22B1560, KME22B1634, KME22B1636, KME22B1694, KME22B1752, KME22B1753, KME22B1793, KME22B1794, KME22B1873, KME22B2124, KME22B2125, KME22B2752, KME22B2884, KME22B2901, KME22C0067, KME22C0241, KME22C0532, KME22C0864, KME22C1020, KME22C1317, KME22C1860, KME22C1942, KME22C2352, KME22C2353, KME22C2649, KME22C2654, KME22C2723, KME22C2859, KME22C2987, KME22C2988, KME22C3185, KME22D0594, KME22D0711, KME22D0716, KME22D0831, KME22D0836, KME22D1498, KME22D1499, KME22D1964, KME22D1965, KME22D2545, KME22D2547, KME22D2548, KME22D2640, KME22D2738, KME22D2847, KME22D2848

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 24 of 123

Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504575

Z-1850-2023
Recall number
Z-1850-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
684042 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 4026704547623, Batch Numbers: 18FG05, 18FG13, 18FG30, 18GG02, 18GG08, 18GG12, 18GG17, 18GG20, 18GG28, 18HG01, 18HG12, 18HG22, 18HG27, 18HG35, 18HG38, 18IG09, 18IG17, 18IG27, 18IG30, 18JG14, 18JG17, 18KG07, 18KG09, 18KG18, 18KG29, 18KG41, 18KG44, 18LG02, 18LG05, 18LG12, 18LG22, 18LG31, 19AG05, 19AG18, 19AG24, 19AG27, 19AG31, 19AG34, 19BG01, 19BG07, 19CT20, 19CT32, 19CT37, 19CT49, 19CT55, 19CT58, 19CT65, 19DT38, 19DT45, 19ET05, 19ET22, 19ET28, 19ET45, 19ET50, 19ET54, 19ET60, 19FT01, 19FT14, 19FT24, 19FT35, 19FT41, 19FT49, 19GT01, 19GT05, 19GT10, 19GT28, 19GT38, 19GT59, 19HT05, 19HT10, 19HT61, 19HT70, 19HT75, 19HT80, 19IT06, 19IT14, 19IT25, 19IT29, 19IT39, 19IT44, 19JT22, 19JT57, 19JT70, 19KT08, 19KT25, 19KT48, 19LT04, 19LT10, 19LT23, 19LT50, 20AT09, 20AT14, 20AT25, 20AT32, 20AT37, 20AT46, 20AT53, 20CT05, 20CT12, 20CT27, 20CT36, 20CT44, 20DT09, 20DT37, 20ET04, 20ET16, 20ET37, 20ET56, 20FT61, 20FT65, 20GT06, 20GT31, 20GT38, 20GT49, KME20H0980, KME20H0981, KME20H1654, KME20H1794, KME20H1848, KME20J0061, KME20J0157, KME20J0322, KME20J0323, KME20J0576, KME20J0829, KME20J0831, KME20J0834, KME20J1114, KME20J2544, KME20K0769, KME20K0770, KME20K1150, KME20K1204, KME20K1665, KME20K2188, KME20K2920, KME20K3016, KME20K3018, KME20K3159, KME20K3575, KME20L1476, KME20L2374, KME20M0383, KME20M1151, KME20M2051, KME20M2344, KME20M2376, KME20M2485, KME20M2556, KME21A0084, KME21A0303, KME21A0671, KME21A0672, KME21A0673, KME21A2799, KME21A2815, KME21G1164, KME21G1165, KME21G1356, KME21G2407, KME21J0947, KME21J1716, KME21J1841, KME21K0659, KME21K1347, KME21K1765, KME21K1844, KME21K2349, KME21K2974, KME21L0634, KME21L0876, KME21L1024, KME21L1392, KME21L2221, KME21L2348, KME21L2765, KME21M0086, KME21M0286, KME21M0363, KME21M0546, KME21M0962, KME21M1889, KME21M2037, KME21M2325, KME21M2564, KME21M2848, KME22A0204, KME22A0546, KME22A1057, KME22A1198, KME22A1514, KME22A1588, KME22A1725, KME22A1727, KME22A1753, KME22A1877, KME22A1912, KME22A2057, KME22A3084, KME22A3086, KME22A3087, KME22A3151, KME22A3270, KME22B0570, KME22B0649, KME22B0850, KME22B1220, KME22B1407, KME22B2126, KME22B2127, KME22B2128, KME22B2162, KME22B2333, KME22B2471, KME22B2472, KME22B2497, KME22B2703, KME22B2903, KME22C0243, KME22C1859, KME22C2294, KME22C2402, KME22C2578, KME22D1474, KME22D2638, KME22D3063, KME22D3064, KME22D3677, KME22G1070, KME22G1071, KME22H2369, KME22H2372, KME22H2630, KME22H2905, KME22J0801, KME22J0802, KME22J2720, KME22J2721, KME22J3353, KME22K0311, KME22K0313

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 25 of 123

Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504580

Z-1851-2023
Recall number
Z-1851-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
244120 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 4026704547630, Batch Numbers: 18FG03, 18FG05, 18FG13, 18GG14, 18HG22, 18HG38, 18IG09, 18JG06, 18JG14, 18JG26, 18KG09, 18KG15, 18KG23, 18LG05, 18LG12, 18LG18, 19AG05, 19AG31, 19BG01, 19BG07, 19CT32, 19CT41, 19CT55, 19DT38, 19DT45, 19DT52, 19ET05, 19ET32, 19ET60, 19ET72, 19ET77, 19FT24, 19GT10, 19GT20, 19GT38, 19GT59, 19HT05, 19IT06, 19JT42, 19JT49, 19KT17, 19LT04, 19LT17, 20AT09, 20AT14, 20AT25, 20AT32, 20AT37, 20AT46, 20AT53, 20BT05, 20BT23, 20BT47, 20CT05, 20CT12, 20CT27, 20CT36, 20CT44, 20DT14, 20DT37, 20ET16, 20ET21, 20GT06, 20GT25, KME20H0590, KME20H0973, KME20H0974, KME20H1289, KME20H1290, KME20H2924, KME20H2926, KME20K0449, KME20K0450, KME20K1414, KME20K2622, KME20L1277, KME20L1479, KME20L2302, KME20L2828, KME20M1752, KME20M1753, KME21A0381, KME21A0820, KME21A0823, KME21D1784, KME21E1286, KME21F1330, KME21J0409, KME21K2402, KME21L0372, KME21L1534, KME21L1899, KME21L2812, KME21M2036, KME21M2053, KME21M2870, KME22A0395, KME22A1237, KME22A3025, KME22A3271, KME22A3272, KME22A3283, KME22A3284, KME22A3285, KME22B1406, KME22B1996, KME22B2164, KME22B2329, KME22B2330, KME22B2496, KME22B2504, KME22B2595, KME22C0247, KME22C0865, KME22C1074, KME22C1321, KME22C1322, KME22H3393, KME22J1538, KME22J1713, KME22J3328, KME22K0537, KME22K0602, KME22K0744, KME22K0760, KME22L1503, KME22L1515, KME22M2049

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 26 of 123

Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504585

Z-1852-2023
Recall number
Z-1852-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
56640 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 4026704547647, Batch Numbers: 18FG13, 18FG15, 18FG25, 18GG20, 18GG28, 18HG12, 18HG19, 18IG06, 18IG27, 18JG02, 18JG23, 18JG26, 18KG18, 18KG23, 19AG05, 19AG31, 19AG37, 19CT17, 19CT58, 19CT71, 19DT02, 19ET32, 19ET45, 19FT14, 19FT24, 19GT52, 19HT61, 19HT80, 19IT39, 19KT17, 19KT48, 19LT50, 20AT32, 20AT53, 20BT05, 20CT12, 20CT44, 20DT09, 20DT37, 20GG27, 20GG45, 20GT38, KME20H0532, KME20J2404, KME20J2405, KME20K2625, KME20L0624, KME20L1482, KME20L2303, KME20L2832, KME21E1295, KME21K1874, KME21M1728, KME21M2447, KME21M2519, KME22B0987, KME22B1754, KME22B2155, KME22C0679, KME22C0866, KME22C2001, KME22C2381, KME22D0823, KME22F1553, KME22F2230, KME22H0145, KME22J0252, KME22J0259, KME22J0470, KME22J2352, KME22L2186, KME22L2295, KME22L2804

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 27 of 123

Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504590

Z-1853-2023
Recall number
Z-1853-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
13710 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 4026704547654, Batch Numbers: 18FG18, 18FG20, 18GG17, 18GT32, 18HG12, 18HG27, 18HG38, 18IG15, 18IG30, 18KG03, 18KG07, 18KG35, 18LG18, 19AG24, 19AG27, 19BG04, 19DT38, 19DT45, 19ET32, 19ET72, 19FT14, 19GT20, 19HT40, 19IT39, 19IT58, 19KT17, 19KT21, 19LT50, 20BG16, 20BT05, 20BT47, 20CT36, 20CT44, KME20H0238, KME20H0239, KME20H0591, KME20J2420, KME21E1114, KME22B1404, KME22B1405, KME22B1755, KME22C0915, KME22C1943, KME22C2372, KME22D1717, KME22D1718, KME22G1443, KME23A2760, KME23C0137

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 28 of 123

Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506525

Z-1854-2023
Recall number
Z-1854-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
17551 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 4026704547661, Batch Numbers: 18FG05, 18FG13, 18GG17, 18GG28, 18HG16, 18HG25, 18HG29, 18HG35, 18HG38, 18IG06, 18IG12, 18IG24, 18IG27, 18JG11, 18JG14, 18JG26, 18JG34, 18KG23, 18LG05, 18LG12, 18LG22, 19AG18, 19AG21, 19AG37, 19CT32, 19CT55, 19ET45, 19GT05, 19GT20, 19GT38, 19GT59, 19HT05, 19HT15, 19HT40, 19HT80, 19IT29, 19KT08, 19KT25, 19KT41, 19KT48, 19LT04, 20AT25, 20AT46, 20BT13, 20BT27, 20CT12, 20CT22, 20CT36, 20CT51, 20DT37, 20ET16, 20ET28, 20FT44, KME20L0615, KME20M2047, KME21A1889, KME21A1890, KME21A2804, KME21B1143, KME21B1672, KME21C0063, KME21C0301, KME21M1833, KME22B0302, KME22B1071, KME22C3357, KME22D0784, KME22D1062, KME22D3648, KME22E1130, KME22F0161, KME22F1501, KME22G0561, KME22G1100, KME22H2626, KME22K0013, KME22K0331, KME22K2365, KME22L0760

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 29 of 123

Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506530

Z-1855-2023
Recall number
Z-1855-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
32553 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 4026704547678, Batch Numbers: 18FG05, 18GG12, 18GG17, 18GG31, 18GT32, 18HG12, 18HG16, 18IG02, 18IG06, 18IG15, 18IG21, 18IG27, 18JG02, 18JG23, 18JG32, 18JG34, 18KG15, 18KG23, 18LG02, 18LG22, 18LG28, 19AG21, 19AG24, 19AG27, 19AG37, 19BG25, 19BG40, 19CT65, 19ET72, 19FT01, 19GT05, 19GT20, 19GT59, 19GT65, 19HT40, 19HT61, 19HT80, 19IT29, 19IT39, 19JT18, 19JT22, 19JT29, 19JT49, 19JT57, 19KT08, 19LT04, 19LT48, 20AT09, 20AT32, 20AT44, 20AT46, 20AT53, 20BT23, 20BT37, 20BT47, 20CT05, 20CT12, 20CT36, 20DT37, 20ET16, 20ET28, KME20J0318, KME20K0152, KME20K0153, KME20K0154, KME20K3587, KME20L1467, KME20L1468, KME20L1838, KME20M2048, KME20M2480, KME21A0669, KME21A1897, KME21A2807, KME21B1674, KME21B1675, KME21C0489, KME21M0865, KME21M2740, KME21M2741, KME22B2144, KME22B2326, KME22B2327, KME22C1075, KME22C1826, KME22C3192, KME22D0787, KME22E0223, KME22E1029, KME22F0563, KME22G0910, KME22G0911, KME22H0780, KME22H2909, KME22J0577, KME22K0015, KME22K0016, KME22K0202, KME22K0335, KME22K0918

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 30 of 123

Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506535

Z-1856-2023
Recall number
Z-1856-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
18353 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 4026704547685, Batch Numbers: 18FG05, 18FG20, 18GG12, 18GG17, 18GG28, 18GT32, 18HG12, 18HG16, 18JG17, 18KG07, 18LG02, 18LG22, 18LG28, 19AG21, 19BG40, 19CT58, 19ET38, 19ET60, 19ET72, 19FT01, 19GT05, 19GT10, 19GT20, 19GT45, 19GT59, 19GT65, 19HT05, 19HT40, 19HT61, 19HT80, 19IT29, 19JT49, 19KT08, 19LT04, 19LT48, 20AT32, 20AT53, 20BT05, 20BT23, 20BT47, 20CT12, 20CT22, 20CT36, 20CT44, 20DT14, 20DT37, 20ET16, 20ET21, 20ET28, 20FT44, KME20K1624, KME20K3589, KME20L0616, KME20L0617, KME20M2049, KME20M3274, KME20M3275, KME20M3278, KME21A1899, KME21A2809, KME21B0575, KME21C0027, KME21C0491, KME22A0057, KME22A0206, KME22B0539, KME22B0725, KME22B1028, KME22B1562, KME22C0916, KME22C1821, KME22C1940, KME22D0350, KME22D1078, KME22F0162, KME22F2162, KME22G3101, KME22G3233, KME22H2624, KME22J0803, KME22J3077

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 31 of 123

Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506540

Z-1857-2023
Recall number
Z-1857-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
16400 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 4026704547692, Batch Numbers: 18FG05, 18FG13, 18FG22, 18GG17, 18GG28, 18GT32, 18HG16, 18JG02, 18JG17, 18JG32, 18JG34, 18KG29, 18KG35, 18LG02, 18LG12, 18LG18, 18LG28, 19AG21, 19BG21, 19BG40, 19ET38, 19ET60, 19ET72, 19FT01, 19FT18, 19FT35, 19GT05, 19GT28, 19HT15, 19HT40, 19HT80, 19IT39, 19JT57, 19LT04, 19LT17, 20AT09, 20AT32, 20AT53, 20BT23, 20CT12, 20CT22, 20CT36, 20ET49, 20ET56, 20GG45, KME20J2322, KME20K0940, KME20K2247, KME20L0621, KME20L1470, KME20L2029, KME20M2093, KME20M2481, KME21A0670, KME21A2814, KME21B1689, KME21B1692, KME22B1078, KME22C1972, KME22C2370, KME22D0541, KME22D0788, KME22E0224, KME22E1238, KME22F0048, KME22G2817

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 32 of 123

Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506545

Z-1858-2023
Recall number
Z-1858-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
12400 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 4026704547708, Batch Numbers: 18FG05, 18FG13, 18GG20, 18HG16, 18IG06, 18IG12, 18JG04, 18JG14, 18JG21, 18JG34, 18KG35, 18LG02, 18LG18, 18LG28, 19BG21, 19CT49, 19FT35, 19GT20, 19GT28, 19GT38, 19GT59, 19GT65, 19HT24, 19HT80, 19IT29, 19KT25, 19KT48, 19LT38, 20AT09, 20BG16, 20BT05, 20CT05, 20CT36, 20CT44, 20DT37, 20GG45, KME20H2927, KME20H2928, KME20K2248, KME20L0620, KME20L1471, KME20L1472, KME20L2030, KME20M2482, KME21A1892, KME21A1893, KME21A2811, KME21B0576, KME22G3102, KME22J2956, KME22K2778, KME22L3057, KME23A2083, KME23B1203

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 33 of 123

Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506550

Z-1859-2023
Recall number
Z-1859-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
10600 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 4026704547715, Batch Numbers: 18FG01, 18FG05, 18FG13, 18GG17, 18GG31, 18HG12, 18HG19, 18JG21, 18JG32, 18KG41, 18LG18, 18LG28, 19AG21, 19DT25, 19DT33, 19ET54, 19ET77, 19FT24, 19GT59, 19GT65, 19HT24, 19HT61, 19IT29, 19JT42, 19JT49, 19JT57, 19KT25, 20AT14, 20AT25, 20AT44, 20BT05, 20BT27, 20BT37, 20BT51, 20CT05, 20CT12, 20CT36, 20DT09, 20ET56, 20GT06, 20GT38, KME20H1790, KME20J2114, KME20J3032, KME20K1344, KME20L1842, KME20L1843, KME20L2299, KME20M2094, KME20M2483, KME21A2812, KME21B1693, KME21C0020, KME22B1976, KME22H3204

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 34 of 123

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 1700100

Z-1860-2023
Recall number
Z-1860-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
190 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 4026704319633, Batch Numbers: 18IG06, 18KG44

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 35 of 123

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180030

Z-1861-2023
Recall number
Z-1861-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
3100 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340436, Batch Numbers: 18GG26, 18GT26, 18JG14, 19AG21, 19CG07, 19CT69, 19DT42, 19ET34, 19FT29, 19HT04, 19IT43, 19KT17, 19LT08, 20DT15, 20DT24, 20ET56, KME20K1810, KME20M0946, KME20M2783, KME21A2389, KME21B0075, KME21B1923, KME22D1514, KME22F2666, KME22G0172, KME22G1751

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 36 of 123

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180035

Z-1862-2023
Recall number
Z-1862-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
4769 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340443, Batch Numbers: 18IG24, 18JG07, 18LG06, 18LG33, 19AG36, 19CT69, 19DT42, 19ET34, 19FT19, 19FT29, 19HT34, 19IT43, 19JT02, 19LT08, 19LT32, 20ET56, KME20K1811, KME20M0947, KME21A0060, KME21A2390, KME21B0599, KME22D1515, KME22G0175, KME22K0607, KME22K3167, KME23A1884

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 37 of 123

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180040

Z-1863-2023
Recall number
Z-1863-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
5120 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340450, Batch Numbers: 18GT26, 18KG10, 18LG33, 19AG21, 19BG12, 19CT36, 19DT42, 19FT29, 19FT49, 20DT24, KME20L2493, KME20M0278, KME21A0061, KME21B1925, KME21M1736, KME22C0700, KME22F0734, KME22G0184, KME22H0033, KME22H3078, KME22J0843

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 38 of 123

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180045

Z-1864-2023
Recall number
Z-1864-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
4155 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340467, Batch Numbers: 18GT26, 18KG10, 18LG06, 19AG11, 19AG21, 19CT69, 19DT06, 19FT29, 19FT49, 19GT43, 19HT66, 19JT55, 19KT17, 19LT08, 19LT32, 20AT49, 20BT53, 20DT15, 20ET04, 20GG27, KME20H2636, KME20K1812, KME20K2573, KME21L2619, KME21M1773, KME22E2900, KME22G0347, KME22J3224, KME22K0489

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 39 of 123

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180050

Z-1865-2023
Recall number
Z-1865-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
4146 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340474, Batch Numbers: 18IG24, 18KG10, 18KG22, 18LG06, 18LG33, 19AG21, 19AG36, 19DT06, 19ET12, 19ET58, 19GT44, 19HT04, 19HT66, 19IT12, 19LT32, 20DT14, 20GG27, KME20J1208, KME21B0077, KME21C0441, KME22D3452, KME22F0736, KME22G0655

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 40 of 123

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180055

Z-1866-2023
Recall number
Z-1866-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
3309 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340481, Batch Numbers: 18IG24, 18JG36, 18LG33, 19AG11, 19AG21, 19DT06, 19ET58, 19FT22, 19FT49, 19HT04, 19HT34, 19HT80, 19IT43, 19JT02, 20AT49, 20BT53, 20CT24, 20DT24, 20GG27, KME20K2673, KME20M0950, KME21A0310, KME21B0602, KME22F0738

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 41 of 123

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180060

Z-1867-2023
Recall number
Z-1867-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
2714 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340498, Batch Numbers: 18KG08, 18LG33, 19AG21, 19BG12, 19ET12, 19FT19, 19HT34, 19IT12, 19IT43, 19LT32, 20AT49, 20DT15, 20GG27, KME20K1813, KME20L2063, KME20M1586, KME21A2393, KME21C3189, KME22D3370, KME22F2673

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 42 of 123

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180065

Z-1868-2023
Recall number
Z-1868-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
1570 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340504, Batch Numbers: 18JG07, 19AG21, 19BG12, 19HT03, 19HT34, 19JT02, 19LT32, 20AT49, KME20M2642, KME21B0078, KME22D1517, KME22H1720, KME22J0807

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 43 of 123

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180070

Z-1869-2023
Recall number
Z-1869-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
970 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340511, Batch Numbers: 18HG40, 18LG33, 19CT36, 19FT19, 19GT46, 19LT31, KME21A2555, KME22H2313, KME22K1045

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 44 of 123

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181030

Z-1870-2023
Recall number
Z-1870-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
2874 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340528, Batch Numbers: 18GG23, 18HG17, 18HG21, 18IG17, 18LG18, 19AG25, 19BG19, 19BG32, 19GT16, 19IT53, 19LT21, KME22F2174, KME22G1753

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 45 of 123

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181040

Z-1871-2023
Recall number
Z-1871-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
12852 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340542, Batch Numbers: 18GG17, 18GG34, 18IG15, 18JG03, 18JG21, 18KG18, 18LG14, 18LG15, 19AG25, 19BG02, 19ET39, 19FT46, 19HT31, 19IT01, 19IT53, 19KT02, 19LT21, 20AT26, 20CT11, 20DT19, 20DT32, KME20J0427, KME20M0303, KME21A2096, KME21A3064, KME21B2620, KME21B2621, KME21C1148, KME21C3436, KME21D0720, KME21D2148, KME21M2369, KME22B0041, KME22B0278, KME22B0588, KME22C0507, KME22D3254, KME22F0607, KME22F2175

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 46 of 123

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181045

Z-1872-2023
Recall number
Z-1872-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
53216 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340559, Batch Numbers: 18FG31, 18FT35, 18GG17, 18GG25, 18GG34, 18HG17, 18IG14, 18JG16, 18JG35, 18JG37, 18KG17, 18KG36, 18KG41, 18LG14, 18LG39, 19AG25, 19BG02, 19BG32, 19CG01, 19CG02, 19CT26, 19CT53, 19CT56, 19CT57, 19DT03, 19DT34, 19DT42, 19ET61, 19GT13, 19GT16, 19GT60, 19HT59, 19LT36, 20AT26, 20CT05, 20CT32, KME21C1880, KME21D0722, KME21D1235, KME21D2149, KME21D2150, KME21L2312, KME21M0208, KME21M0957, KME21M0958, KME21M0959, KME21M2377, KME21M2379, KME22B0281, KME22B1307, KME22B1308, KME22B1464, KME22C0411, KME22C2193, KME22D1004, KME22D1005, KME22E1405, KME22E1503, KME22E2767, KME22F0777, KME22F1313, KME22F2624, KME22G0321, KME22G1706, KME22G2273, KME22H0491, KME22H1075, KME22H1324, KME22J0385

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 47 of 123

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181050

Z-1873-2023
Recall number
Z-1873-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
54469 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340566, Batch Numbers: 18FG31, 18FT35, 18GG23, 18GT32, 18HG17, 18JG19, 18JG21, 18JG37, 18KG18, 18KG19, 18KG21, 18KG38, 18KG39, 18LG14, 19AG01, 19BG02, 19BG18, 19CG01, 19CG02, 19CT28, 19DT05, 19DT30, 19DT35, 19ET36, 19ET39, 19ET40, 19ET61, 19ET69, 19FT01, 20AT26, 20DT18, KME21A2039, KME21B2623, KME21C0543, KME21C1149, KME21C3398, KME21C3399, KME21D1236, KME21F0888, KME21L2303, KME21L2790, KME21M2313, KME21M2314, KME21M2317, KME21M2318, KME21M2380, KME21M2481, KME22A0760, KME22A2297, KME22B0755, KME22B2679, KME22C0412, KME22C2194, KME22C2195, KME22D1145, KME22D2262, KME22D3177, KME22F1334, KME22F2203, KME22F3000, KME22F3239, KME22F3241

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 48 of 123

Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382030

Z-1874-2023
Recall number
Z-1874-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
25160 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340795, Batch Numbers: 18FT13, 18GT32, 18HG08, 18HG25, 18IG29, 18JG35, 18KG08, 18LG23, 19AG08, 19AG23, 19AG38, 19BG12, 19BG35, 19CT37, 19CT42, 19DT36, 19ET51, 19FT08, 19GT05, 19GT35, 19IT11, 19IT56, 19KT13, 19LT27, 20AT05, 20BT43, 20CT07, 20DT22, 20ET30, 20FT43, 20FT55, 20GT18, KME20K0276, KME20M3220, KME21A0764, KME21C0890, KME21C1020, KME21C1033, KME21C1572, KME21C2686, KME21D1293, KME21D1448, KME21D1743, KME21D1913, KME21F0962, KME22A2454, KME22C1763, KME22D2425, KME22D2823, KME22E0291, KME22E0560, KME22E2506, KME22E2684, KME22E2925, KME22F1606, KME22J1478, KME22K0878, KME22L2920, KME22M0084, KME22M0213

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 49 of 123

Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382035

Z-1875-2023
Recall number
Z-1875-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
25435 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340801, Batch Numbers: 18GG15, 18GT32, 18IG13, 18KG24, 18KG33, 18KG34, 18LG01, 18LG03, 19CG05, 19CT36, 19CT72, 19DT13, 19KT20, 20AT05, 20AT50, 20BG19, 20BT43, 20DT01, 20DT04, 20DT24, 20ET30, 20FT21, 20FT43, 20FT58, 20FT68, 20GT22, KME20G0092, KME20K0870, KME20L1581, KME20L1894, KME20M3043, KME21B0039, KME21B1553, KME21C0891, KME21C0930, KME21C1580, KME21L2524, KME22B0933, KME22C2632, KME22C2804, KME22D1106, KME22D2022, KME22D2157, KME22D2462, KME22D2650, KME22D3220, KME22D3334, KME22E0292, KME22E0669, KME22E2685, KME22E2686, KME22F1707, KME22F2556, KME22H1215, KME22J2124, KME22K0712, KME22K0713, KME22K1577, KME22K2171, KME22K2382, KME22K2545, KME22L1846, KME22L2147, KME22L2341, KME22L2372, KME22L2411, KME22M1269, KME22M2426

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 50 of 123

Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382050

Z-1876-2023
Recall number
Z-1876-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
12382 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340832, Batch Numbers: 18FG02, 18FT26, 18FT35, 18GG26, 18HT18, 18IG04, 18IG10, 18JG36, 18JT06, 18JT10, 18KG23, 18KT30, 18LG06, 18LT18, 19BG16, 19BG21, 19CG06, 19DT16, 19DT39, 19GT58, 19IT20, 19JT46, 19KT29, 19LT46, 20AT26, 20CT11, 20CT38, 20DT13, 20DT23, 20GG45, 20GT24, 20GT41, 20GT44, KME20H0293, KME20H1490, KME20H2049, KME20L1755, KME20L2383, KME20L2596, KME20M2056, KME21M2476, KME22A1524, KME22D0857, KME22D2479, KME22D3022, KME22F2427, KME22G0200, KME22G1191

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 51 of 123

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780075

Z-1877-2023
Recall number
Z-1877-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
15810 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341112, Batch Numbers: 18FG21, 18FG31, 18GG19, 18HG23, 18HG30, 18IG16, 18IG30, 18JG35, 18KG19, 18KG41, 18LG18, 19AG03, 19BG04, 19BG19, 19CG03, 19CT36, 19DT34, 19FT37, 19GT65, 19HT55, 19IT01, 19IT19, 19JT38, 19LT21, 20AT26, 20BG11, 20CT12, 20DT22, 20ET04, 20ET49, 20FT65, KME20H0627, KME20K0991, KME20K3625, KME20L2680, KME21A1113, KME21A2088, KME21A3085, KME21B0714, KME21B2708, KME21C0596, KME21C1167, KME21L0761, KME21L0859, KME22A1383, KME22B2543, KME22B2906, KME22D0652, KME22D3251, KME22E1151, KME22E1506, KME22G0386, KME22G3151, KME22G3270, KME22H2700, KME22J0257, KME22J1105, KME22J1335, KME22K3101, KME22M1594

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 52 of 123

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781040

Z-1878-2023
Recall number
Z-1878-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
347422 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341167, Batch Numbers: 18FT35, 18GG16, 18GG19, 18GG23, 18GG34, 18GT32, 18HG17, 18HG21, 18HG22, 18HG29, 18HG30, 18IG15, 18JG01, 18JG03, 18JG16, 18JG19, 18JG35, 18JG37, 18KG17, 18KG19, 18KG38, 18LG12, 18LG14, 18LG18, 18LG30, 19AG01, 19AG19, 19AG29, 19BG18, 19BG32, 19BG33, 19CG01, 19CG02, 19CT26, 19CT33, 19CT53, 19CT73, 19CT80, 19CT82, 19DT05, 19DT30, 19DT35, 19DT38, 19DT42, 19ET18, 19ET34, 19ET39, 19ET40, 19ET58, 19ET60, 19ET61, 19ET65, 19ET69, 19FT01, 19FT41, 19GT13, 19GT16, 19GT63, 19HT31, 19HT82, 19IT01, 19IT14, 19JT35, 19JT56, 19JT63, 19KT02, 19KT41, 19KT46, 19LT21, 19LT36, 20AT22, 20AT53, 20BT01, 20BT02, 20CT05, 20DT23, 20DT29, 20DT32, 20DT35, 20ET04, 20ET33, 20ET34, 20ET38, 20ET39, 20FT17, 20FT19, 20FT60, 20FT64, 20FT68, 20GT11, 20GT34, KME20H1786, KME20H2999, KME20J0367, KME20J0494, KME20J1209, KME20J1388, KME20M2796, KME20M2906, KME20M2907, KME20M2994, KME20M3092, KME21A1005, KME21A1006, KME21A2030, KME21A2037, KME21A3023, KME21A3024, KME21A3028, KME21A3029, KME21B0259, KME21B0788, KME21B0994, KME21B1198, KME21B1286, KME21B1288, KME21B1620, KME21B2627, KME21B2628, KME21B2705, KME21C0428, KME21C1121, KME21C1199, KME21C1879, KME21C3336, KME21F0980, KME21K1094, KME21K1655, KME21K1714, KME21K1841, KME21K2300, KME21K3006, KME21L2290, KME21L2744, KME21L2745, KME21L2760, KME21L2761, KME21L2787, KME21L2869, KME21M0203, KME21M0801, KME21M0809, KME21M0950, KME21M1706, KME21M1904, KME21M1905, KME21M2908, KME22A0561, KME22A2283, KME22A2404, KME22A2849, KME22A2915, KME22A3199, KME22B0002, KME22B0003, KME22B0004, KME22B0043, KME22B0123, KME22B0124, KME22B0165, KME22B0192, KME22B0545, KME22B0585, KME22B1999, KME22C1877, KME22C1989, KME22C1990, KME22C2189, KME22C2479, KME22C2480, KME22C2481, KME22C2659, KME22C2660, KME22C2760, KME22C2839, KME22C2840, KME22C2866, KME22C2966, KME22C3124, KME22C3126, KME22C3454, KME22D0284, KME22D1566, KME22D1674, KME22D1698, KME22D1813, KME22D1890, KME22D2708, KME22D3011, KME22E0730, KME22E0731, KME22E0945, KME22E1105, KME22E1394, KME22E1499, KME22E1933, KME22E2376, KME22E2659, KME22E2810, KME22E2889, KME22F0001, KME22F0541, KME22F2997, KME22F3120, KME22F3243, KME22F3423, KME22G0815, KME22G1098, KME22G1167, KME22G1228, KME22G1229, KME22G1330, KME22G2240, KME22G2307, KME22G2576, KME22G2629, KME22G2924, KME22G3134, KME22H0545, KME22H0600, KME22H0761, KME22H1361, KME22H1725, KME22H1932, KME22H2056, KME22H2520, KME22H3068

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 53 of 123

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781045

Z-1879-2023
Recall number
Z-1879-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
446163 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341174, Batch Numbers: 18FG33, 18GG16, 18HG17, 18HG21, 18HG29, 18HG30, 18HG31, 18IG10, 18IG14, 18IG17, 18IG20, 18JG02, 18JG03, 18JG16, 18JG19, 18JG20, 18JG35, 18JG37, 18KG01, 18KG17, 18KG19, 18KG36, 18KG39, 18KG41, 18LG12, 18LG14, 18LG30, 18LG39, 19AG01, 19AG17, 19AG19, 19AG29, 19BG02, 19BG18, 19BG19, 19BG32, 19BG33, 19CG01, 19CT26, 19CT33, 19CT53, 19CT56, 19CT80, 19DT05, 19DT30, 19DT46, 19ET18, 19ET34, 19ET39, 19ET40, 19ET61, 19ET65, 19ET69, 19FT01, 19FT41, 19GT13, 19HT68, 19IT01, 19IT15, 19IT53, 19IT54, 19JT06, 19JT10, 19JT14, 19JT56, 19JT63, 19KT02, 19KT14, 19KT38, 19KT41, 19LT16, 19LT21, 19LT36, 20AT22, 20BT02, 20CT02, 20CT05, 20CT11, 20CT14, 20CT32, 20DT19, 20DT20, 20DT23, 20DT29, 20DT32, 20DT35, 20ET33, 20ET34, 20ET38, 20ET39, 20ET49, 20FT17, 20FT18, 20FT60, 20GT34, KME20H0612, KME20H1787, KME20H2570, KME20H2572, KME20H2573, KME20H3001, KME20H3127, KME20H3128, KME20J1211, KME20J1389, KME21A1007, KME21A1008, KME21A1182, KME21A2025, KME21A2026, KME21A2189, KME21A3059, KME21A3060, KME21A3083, KME21A3084, KME21B0258, KME21B0790, KME21B1083, KME21B1259, KME21B1289, KME21B1545, KME21B1605, KME21B1754, KME21B2217, KME21B2530, KME21B2672, KME21C0424, KME21C0425, KME21C2416, KME21J1495, KME21K1633, KME21K1715, KME21K1842, KME21K1866, KME21K2302, KME21K2458, KME21K2459, KME21K2495, KME21K2579, KME21K2998, KME21K3000, KME21K3001, KME21L0074, KME21L0890, KME21L1033, KME21L1359, KME21L1364, KME21L1365, KME21L1435, KME21L1525, KME21L2143, KME21L2788, KME21M0949, KME21M1654, KME21M1655, KME21M1656, KME21M1906, KME21M1907, KME21M2271, KME21M2424, KME21M2479, KME21M2674, KME21M2706, KME21M2909, KME22A0562, KME22A1471, KME22A2179, KME22A2917, KME22A3198, KME22A3264, KME22B0005, KME22B0167, KME22B0191, KME22B0239, KME22B0277, KME22B0358, KME22B0399, KME22B0502, KME22B0580, KME22B1038, KME22B1144, KME22B1145, KME22B1224, KME22B1265, KME22B1309, KME22B1341, KME22B1418, KME22C0060, KME22C0494, KME22C0791, KME22C0792, KME22C1080, KME22C1081, KME22C1082, KME22C1236, KME22C1237, KME22C1472, KME22C1710, KME22C1711, KME22C1724, KME22C1850, KME22C1852, KME22C1878, KME22C1879, KME22C1880, KME22C1991, KME22C1992, KME22C2190, KME22C2968, KME22D0091, KME22D0153, KME22D0248, KME22D0285, KME22D0321, KME22D0444, KME22D0536, KME22D0717, KME22D1659, KME22D2057, KME22D2469, KME22D3211, KME22E1501, KME22E1932, KME22E2026, KME22E2122, KME22E2690, KME22E2805, KME22E2888, KME22E2928, KME22F0230, KME22F2072, KME22F2355, KME22F2625, KME22F3383, KME22F3502, KME22G0215, KME22G0234, KME22G0262, KME22G0476, KME22G0537, KME22G0735, KME22G0788, KME22G1047, KME22G1109, KME22G1332, KME22G1466, KME22G2049, KME22G2244, KME22G2774, KME22H1202

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 54 of 123

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781075

Z-1880-2023
Recall number
Z-1880-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
17840 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341235, Batch Numbers: 18FG21, 18GG18, 18GG19, 18HG29, 18IG17, 18JG03, 18JG20, 18JG35, 18KG01, 18KG43, 18LG18, 19AG25, 19BG03, 19BG18, 19BG20, 19DT38, 19ET36, 19FT02, 19HT55, 19HT68, 19IT53, 19LT36, 20AT26, 20BG11, 20CT11, 20DT19, 20FT64, 20GT11, 20GT34, KME20J1216, KME20K3678, KME20L0953, KME20M1291, KME21A1263, KME21A2084, KME21B1948, KME21B1950, KME21C1040, KME21C1041, KME21C2485, KME21C3404, KME21F0144, KME21F1428, KME21K1054, KME21K2543, KME21L2839, KME22A0811, KME22A1220, KME22A2928, KME22B0589, KME22B2683, KME22C2313, KME22D0105, KME22D0296, KME22D0589, KME22D3070, KME22E1853, KME22E2748, KME22F0603, KME22G0210, KME22G1168, KME22H1123, KME22H3070, KME22J1084, KME22K2080, KME22K2470, KME22L0201, KME22L0202, KME23A1196

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 55 of 123

Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080055

Z-1881-2023
Recall number
Z-1881-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
2520 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341266, Batch Numbers: 18FG02, 18IG29, 18KG28, 19AG39, 19BG02, 19CT64, 19GT31, 19IT33, 20DT18, KME20G0435, KME20K2579, KME21K0764, KME21K1278, KME22B0079, KME22B0080, KME22E2802, KME22H2250

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 56 of 123

Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080095

Z-1882-2023
Recall number
Z-1882-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
760 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341266, Batch Numbers: 18IT25, 18JG13, 19CT66, 19HT79, 19KT08, 20BT13, 20DT19, KME22C0673

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 57 of 123

Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080100

Z-1883-2023
Recall number
Z-1883-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
690 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341266, Batch Numbers: 18FT26, 18IT18, 18KG10, 19CG03, 19IT31, 20BT13, 20DT18, 20GT57, KME22C0947

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 58 of 123

Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082050

Z-1884-2023
Recall number
Z-1884-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
47520 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341389, Batch Numbers: 18GG02, 18GG19, 18GG23, 18GT06, 18JG04, 18JG15, 18JG16, 18JG18, 18JT06, 18JT16, 19AG33, 19AT20, 19BG02, 19BG03, 19BG10, 19BG15, 19BG22, 19BG26, 19BG42, 19BT04, 19CT25, 19CT82, 19DT05, 19FT38, 19IT26, 19JT18, 19LT13, 19LT17, 19LT50, 20AT13, 20AT40, 20BT38, 20CT02, 20CT12, 20CT43, 20DT13, 20ET12, 20ET17, 20ET56, 20FT23, 20GG47, 20GT32, KME20J1385, KME21G1704, KME21G1949, KME21K0151, KME21K0292, KME21M2075, KME21M2306, KME21M2649, KME22A1589, KME22A2197, KME22B1848, KME22B2478, KME22B2538, KME22B2578, KME22B2692, KME22C0066, KME22C0571, KME22D0281, KME22D2503, KME22D2504, KME22E0316, KME22E1277, KME22E1422, KME22E2743, KME22E2879, KME22G0063, KME22J0616, KME22J1331, KME22J1463, KME22K0660, KME22L1657, KME23A2133, KME23A2214, KME23A2221, KME23A2299, KME23A2358, KME23C0172

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 59 of 123

Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082055

Z-1885-2023
Recall number
Z-1885-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
49050 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341396, Batch Numbers: 18FG33, 18FT26, 18GG13, 18GG15, 18GG25, 18GT11, 18GT34, 18HG28, 18IG05, 18IG14, 18JT04, 18KG25, 18KG26, 18LG19, 18LG40, 19AG19, 19AG32, 19AG33, 19ET31, 19ET73, 19JT36, 19KT18, 20AT32, 20AT40, 20BT10, 20BT38, 20CT54, 20ET17, 20ET18, KME20G0395, KME20H0640, KME20J2829, KME20L1703, KME21A1433, KME21E0864, KME21E1230, KME21F0946, KME21F1967, KME21G0850, KME21J0319, KME21K1627, KME21M0312, KME22A2333, KME22A2942, KME22B0352, KME22B0563, KME22B1357, KME22C0323, KME22C2218, KME22C2923, KME22D0055, KME22D0282, KME22D0603, KME22D1799, KME22D3018, KME22E0652, KME22E1164, KME22F0418, KME22F0898, KME22F1662, KME22G0318, KME22G2350, KME22H0635, KME22H1516, KME22H1612, KME22J1044, KME22J1464, KME22J2331, KME22J2332, KME22K0635, KME22K0780, KME22K1440, KME23A2300, KME23A2432, KME23A2845, KME23A3010

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 60 of 123

Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082060

Z-1886-2023
Recall number
Z-1886-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
170610 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341402, Batch Numbers: 18GG13, 18GG15, 18HG07, 18HG30, 18IG06, 18IG14, 18IG27, 18IT06, 18IT18, 18IT25, 18JT06, 19CG03, 19CT25, 19CT29, 19CT45, 19CT50, 19CT61, 19CT76, 19DT05, 19DT14, 19GT07, 19HT61, 19IT05, 19IT12, 19IT33, 19IT43, 19IT55, 19IT59, 19JT30, 19KT07, 19KT31, 19LT04, 19LT08, 20AT41, 20AT49, 20BT39, 20BT46, 20BT51, 20CT13, 20CT54, 20ET12, 20ET15, 20ET16, 20ET17, 20FT23, 20FT45, 20GT09, 20GT34, 20GT38, KME20J0548, KME20J1458, KME20J2801, KME20K0435, KME20K1112, KME20K2168, KME20L1143, KME20L1420, KME20L2089, KME20L2783, KME20M0663, KME20M1064, KME20M1143, KME21E0660, KME21G0572, KME21G1976, KME21G2260, KME21H0911, KME21H1123, KME21K0411, KME21K0550, KME21L0214, KME21L0952, KME21L2133, KME21L2271, KME21M2791, KME21M2792, KME22A1454, KME22A1518, KME22A2004, KME22A2431, KME22A2484, KME22A2892, KME22A2958, KME22B0288, KME22B0499, KME22B1509, KME22B1895, KME22C0832, KME22D2180, KME22D3181, KME22E0328, KME22E0977, KME22F0005, KME22F0189, KME22F0762, KME22F1398, KME22F2154, KME22F3471, KME22G0140, KME22G0188, KME22G2351, KME22G2656, KME22G3065, KME22G3236, KME22H0773, KME22H0828, KME22H1589, KME22J1998, KME22K0733, KME22K0898, KME22K0991, KME23B0877

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 61 of 123

Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082065

Z-1887-2023
Recall number
Z-1887-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
247645 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341419, Batch Numbers: 18FG23, 18FG27, 18FG30, 18FG31, 18FT06, 18FT08, 18GG19, 18GT32, 18GT34, 18HG02, 18HG15, 18IG02, 18IG07, 18IG13, 18IT25, 18JG01, 18JG02, 18JG04, 18JG07, 18JG20, 18KG44, 18KT28, 18LG14, 19AG09, 19AG15, 19AG32, 19AG33, 19AT20, 19BG14, 19BG18, 19BG40, 19CG07, 19CT26, 19CT39, 19CT40, 19CT76, 19DT10, 19DT16, 19DT27, 19DT47, 19ET02, 19ET05, 19ET65, 19GT19, 19GT29, 19GT30, 19GT31, 19GT38, 19HT26, 19HT61, 19HT66, 19HT68, 19IT20, 19IT33, 19IT59, 19JT18, 19JT19, 19JT26, 19JT32, 19JT36, 19JT49, 19JT63, 19KT20, 19KT21, 19KT26, 19LT07, 19LT31, 19LT46, 20AT05, 20AT06, 20AT20, 20AT47, 20AT49, 20BT13, 20CT02, 20CT13, 20CT23, 20CT37, 20CT47, 20CT54, 20DT01, 20DT02, 20ET16, 20ET18, 20GT05, 20GT06, 20GT13, 20GT22, 20GT24, KME20H0882, KME20H2726, KME20H2934, KME20J1386, KME20J1399, KME20J1656, KME20K0036, KME20K0259, KME20K0436, KME20K0504, KME20K0677, KME20K0881, KME20L2349, KME20L2447, KME20L2448, KME20M0710, KME20M0892, KME20M0928, KME20M1806, KME20M1923, KME20M2249, KME20M2450, KME20M2708, KME21A0338, KME21A0404, KME21A0695, KME21B1352, KME21B2607, KME21B2789, KME21C0504, KME21C0981, KME21C0983, KME21C1035, KME21C1097, KME21E0607, KME21E0685, KME21F0384, KME21F0516, KME21F0694, KME21F0834, KME21F0930, KME21F1554, KME21F1885, KME21F2156, KME21F2203, KME21G0532, KME21H0202, KME21H0916, KME21H1233, KME21H1264, KME21J0302, KME21J0389, KME21J0528, KME21J0637, KME21J0725, KME21J0909, KME21J1871, KME21J1945, KME21J1998, KME21K0570, KME21K0587, KME21K0829, KME21L0344, KME21L0408, KME21L0566, KME21L1306, KME21L2132, KME21L2653, KME21M0853, KME21M1380, KME21M1469, KME22A0676, KME22A1234, KME22A1388, KME22A1505, KME22A2005, KME22A2059, KME22A2198, KME22A2316, KME22A2350, KME22A2401, KME22A2481, KME22A2694, KME22A2959, KME22A3224, KME22B0070, KME22B0466, KME22B0566, KME22B0946, KME22B1049, KME22B1945, KME22B2102, KME22B2322, KME22B2644, KME22C2076, KME22D0407, KME22D0573, KME22D0810, KME22D1482, KME22D1780, KME22D2011, KME22D2630, KME22D3020, KME22E1854, KME22E2488, KME22F1264, KME22F2116, KME22F2172, KME22F2296, KME22F2720, KME22G0552, KME22G2426, KME22G2943, KME22H0766, KME22H1917, KME22H2054

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 62 of 123

Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082070

Z-1888-2023
Recall number
Z-1888-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
860472 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341426, Batch Numbers: 18FG12, 18GG07, 18GG08, 18GG10, 18GG12, 18GG19, 18GG22, 18GT07, 18GT08, 18GT12, 18HG28, 18HG34, 18HT07, 18HT08, 18HT31, 18IG01, 18IG04, 18IG07, 18IG09, 18IG10, 18IG11, 18IG15, 18IG16, 18IG23, 18IT18, 18IT23, 18JG04, 18KG07, 18KG10, 18KG25, 18KT03, 18LG11, 18LG35, 18LG40, 19AG02, 19AG03, 19AT16, 19BG02, 19BG14, 19BG16, 19BG19, 19BG21, 19BG22, 19BG23, 19BG26, 19BG33, 19BG34, 19BG37, 19BG42, 19BT12, 19BT16, 19BT18, 19CG01, 19CG03, 19CG06, 19CT03, 19CT22, 19CT82, 19DT17, 19DT20, 19DT29, 19DT36, 19DT46, 19DT47, 19ET02, 19ET11, 19ET12, 19ET18, 19ET29, 19ET31, 19ET36, 19ET40, 19ET47, 19ET49, 19ET78, 19ET82, 19FT04, 19FT38, 19FT50, 19GT38, 19GT47, 19GT59, 19GT65, 19HT08, 19HT14, 19HT22, 19HT23, 19HT25, 19HT47, 19HT50, 19HT52, 19HT66, 19HT82, 19IT02, 19IT04, 19IT15, 19IT31, 19KT30, 19KT31, 19LT37, 20AT05, 20AT11, 20AT25, 20AT26, 20AT27, 20AT32, 20AT38, 20AT49, 20BG14, 20BT02, 20BT13, 20BT22, 20BT27, 20BT31, 20BT37, 20BT38, 20BT46, 20BT51, 20BT52, 20BT53, 20CT07, 20DT23, 20DT40, 20ET12, 20ET15, 20ET17, 20FT27, 20FT34, 20FT39, 20FT43, 20FT45, 20FT53, 20FT66, 20FT71, 20GT09, 20GT12, 20GT18, 20GT31, 20GT32, KME20H0916, KME20H1131, KME20H1244, KME20H1245, KME20H1634, KME20J2874, KME20J2896, KME20J2901, KME20J2942, KME20J3266, KME20K0061, KME20K0462, KME20K0585, KME20K1007, KME20K3013, KME20K3014, KME20K3145, KME20K3365, KME20L1691, KME20L1752, KME20L1858, KME20L2111, KME20L2210, KME20L2373, KME20L2463, KME20L2478, KME20L2499, KME20L2699, KME20M0490, KME21B2898, KME21D1652, KME21D1878, KME21D2020, KME21D2929, KME21D2935, KME21E0001, KME21E0002, KME21F0239, KME21F0434, KME21F1379, KME21F1887, KME21F2153, KME21G0013, KME21G0662, KME21G1616, KME21G1663, KME21G1923, KME21G1957, KME21G2511, KME21H0975, KME21H1183, KME21H1265, KME21J0157, KME21J0238, KME21J0497, KME21J0639, KME21J0756, KME21J0774, KME21J0855, KME21J1012, KME21J1207, KME21J1256, KME21J1540, KME21J1605, KME21J1885, KME21J2157, KME21K0003, KME21K0201, KME21K0241, KME21K0388, KME21K0635, KME21K0931, KME21K1129, KME21K1202, KME21K1334, KME21K1415, KME21K1557, KME21K1618, KME21K1816, KME21K2169, KME21K2270, KME21K2533, KME21K2746, KME21K3010, KME21L1055, KME21L1187, KME21L1279, KME21L1367, KME21L1930, KME21M0850, KME21M1390, KME21M1611, KME21M1634, KME21M1698, KME21M1726, KME21M1746, KME21M1864, KME21M1909, KME21M2007, KME21M2032, KME21M2072, KME21M2116, KME21M2147, KME21M2321, KME21M2363, KME21M2700, KME21M2727, KME21M2732, KME21M2744, KME21M3138, KME21M3224, KME21M3225, KME21M3274, KME22A0046, KME22A0224, KME22A0247, KME22A0356, KME22A0429, KME22A0513, KME22A0552, KME22A0621, KME22A0991, KME22A0992, KME22A1045, KME22A1133, KME22A2963, KME22A3194, KME22B0630, KME22B1947, KME22B2203, KME22B2316, KME22B2410, KME22B2585, KME22C1342, KME22C2121, KME22C2755, KME22C2854, KME22C3272, KME22D0480, KME22D1175, KME22D1826, KME22D2302, KME22D2405, KME22D3021, KME22D3274, KME22D3673, KME22D3674, KME22E0177, KME22E0317, KME22E0640, KME22E0655, KME22E0980, KME22E1974, KME22E2559, KME22E2560, KME22E2809, KME22E2919, KME22F0279, KME22F0523, KME22F0792, KME22F0870, KME22F2117, KME22F2905, KME22G0787, KME22G0800, KME22G0809, KME22G1036, KME22J1685, KME22J3142, KME22J3155, KME22J3259, KME22J3276, KME22J3403, KME22K0407, KME22K0509, KME22K2064, KME22K2267

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 63 of 123

Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082075

Z-1889-2023
Recall number
Z-1889-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
300613 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341433, Batch Numbers: 18FG29, 18GG13, 18GG15, 18GG26, 18GT32, 18GT34, 18HG14, 18HG21, 18HG23, 18HG24, 18HG27, 18HT15, 18HT31, 18IG25, 18IG29, 18IT04, 18IT23, 18IT25, 18JG10, 18JT22, 18KG05, 18KT11, 18LG19, 18LG38, 18LG40, 18LT07, 19AG21, 19BG01, 19BG04, 19BG06, 19BG37, 19BT04, 19BT12, 19BT18, 19CG04, 19CG06, 19CT03, 19CT04, 19CT20, 19CT26, 19CT34, 19CT42, 19CT50, 19CT57, 19CT64, 19CT69, 19DT10, 19DT34, 19DT36, 19DT42, 19ET02, 19ET06, 19ET08, 19ET22, 19ET29, 19ET34, 19ET36, 19ET70, 19ET72, 19ET82, 19FT04, 19FT25, 19FT33, 19GT02, 19GT14, 19GT16, 19GT25, 19GT29, 19GT64, 19HT03, 19HT09, 19HT15, 19HT71, 19IT12, 19IT13, 19IT41, 19IT42, 19IT45, 19JT11, 19JT14, 19KT26, 19KT35, 19KT48, 19KT49, 19LT07, 19LT23, 19LT31, 19LT35, 19LT54, 20AT11, 20AT20, 20AT22, 20AT26, 20AT47, 20AT58, 20BT01, 20BT25, 20BT31, 20BT39, 20BT50, 20BT51, 20CT42, 20CT43, 20CT51, 20CT53, 20CT54, 20DT01, 20DT32, 20DT37, 20ET12, 20FT35, 20FT36, 20FT39, 20FT43, 20FT49, 20FT53, 20FT55, 20FT71, 20GG41, 20GG42, 20GT10, 20GT11, 20GT14, 20GT25, 20GT41, 20GT51, 20GT57, KME20J2944, KME20J2988, KME20K1113, KME20L1298, KME20L1299, KME20L1704, KME20L1924, KME20L1983, KME20L2605, KME20L2798, KME20M0034, KME20M0321, KME20M1067, KME20M1507, KME21A3004, KME21A3259, KME21B0179, KME21B0823, KME21B2480, KME21C0615, KME21C0661, KME21C0730, KME21C0826, KME21C0855, KME21C2026, KME21D1923, KME21D1956, KME21D2014, KME21D2018, KME21D2262, KME21E0021, KME21E0288, KME21E0469, KME21E0498, KME21E1186, KME21E1264, KME21F0385, KME21F0557, KME21F0725, KME21F1583, KME21F1607, KME21F1696, KME21F1751, KME21F2182, KME21G0114, KME21G0169, KME21G1942, KME21H0829, KME21J0200, KME21J0359, KME21J0418, KME21J0671, KME21J0763, KME21J1212, KME21J1709, KME21J1842, KME21K0305, KME21K0986, KME21K1712, KME21K1855, KME21K2531, KME21K2745, KME21L0628, KME21L0880, KME21L1025, KME21L1443, KME21L1581, KME21L1663, KME21L1698, KME21L1992, KME21L2222, KME21L2455, KME21L2775, KME21M0193, KME21M0314, KME21M0500, KME21M0690, KME21M0802, KME21M0852, KME21M1006, KME21M1065, KME21M1085, KME21M1245, KME21M1268, KME21M1583, KME21M1613, KME21M1749, KME21M2745, KME21M2871, KME22A0545, KME22A0854, KME22A0940, KME22A1136, KME22A1224, KME22A1367, KME22A1392, KME22A1990, KME22A2129, KME22A2315, KME22A2414, KME22A2537, KME22A2602, KME22A2603, KME22A2898, KME22A2937, KME22A3082, KME22A3219, KME22A3222, KME22A3238, KME22B0266, KME22C2126, KME22C2350, KME22C2437, KME22C2439, KME22C2756, KME22C2855, KME22C3145, KME22D0324, KME22D0464, KME22D1176, KME22D1481, KME22D1660, KME22D1688, KME22D2635, KME22D2853, KME22D3116, KME22D3236, KME22D3419, KME22D3420, KME22D3711, KME22E0179, KME22E0319, KME22E0321, KME22E0322, KME22E0641, KME22E0642, KME22E2647, KME22E3002, KME22F0185, KME22F0317, KME22F0775, KME22F1265, KME22F2028, KME22F2237, KME22F2721, KME22J1258, KME22J3143, KME22J3344

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 64 of 123

Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082080

Z-1890-2023
Recall number
Z-1890-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
170179 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341440, Batch Numbers: 18GG11, 18GG12, 18GG13, 18GT08, 18GT11, 18HG40, 18IG04, 18IG07, 18IG12, 18IG13, 18IG23, 18IT06, 18IT10, 18IT16, 18JG07, 18JG09, 18JG13, 18JG26, 18JG37, 18JG38, 18JT06, 18JT10, 19AG35, 19AG38, 19AT20, 19BG06, 19BG07, 19BG14, 19BG18, 19BG22, 19BG25, 19BG30, 19BT08, 19BT12, 19DT36, 19DT43, 19ET22, 19ET27, 19ET82, 19ET83, 19FT04, 19FT13, 19FT26, 19FT28, 19KT14, 19LT46, 19LT47, 19LT51, 20AT22, 20AT49, 20BG15, 20BG19, 20BT05, 20BT09, 20BT10, 20BT24, 20CT42, 20CT48, 20CT54, 20DT10, 20DT23, 20DT28, 20ET16, 20ET17, 20ET39, 20FT17, 20FT43, 20FT49, 20FT58, 20FT61, 20GG48, 20GT10, 20GT11, 20GT12, 20GT23, KME20G0436, KME20H0953, KME20L1706, KME20L2207, KME20L2333, KME20L2607, KME20L2696, KME20M1043, KME20M1342, KME21A1435, KME21A1524, KME21A2058, KME21B0616, KME21D1653, KME21D1946, KME21D2011, KME21D2012, KME21E0584, KME21E0687, KME21E1452, KME21F0981, KME21F1006, KME21F1215, KME21F1530, KME21F1604, KME21G0736, KME21G1100, KME21J0109, KME21J0563, KME21J1295, KME21J1364, KME21J1415, KME21J1532, KME21J2055, KME21K0022, KME21K0187, KME21K0449, KME21K2884, KME21K3013, KME21L0744, KME21L1438, KME21L1533, KME21L1661, KME21L1787, KME21L2012, KME21L2177, KME21M3032, KME21M3137, KME21M3236, KME22A0626, KME22A0793, KME22A1043, KME22A1701, KME22A2203, KME22A2429, KME22A2693, KME22A2966, KME22B0500, KME22B0737, KME22B0898, KME22B0915, KME22B0991, KME22C1987, KME22C2072, KME22C2219, KME22C2400, KME22C3376, KME22D0004, KME22D1589, KME22D1689, KME22D1897, KME22D2014, KME22D2505, KME22D2636, KME22D3062, KME22D3275, KME22D3421, KME22D3427, KME22D3712, KME22E2014, KME22F0621, KME22F2238, KME22J3346, KME22K0540, KME22K0541, KME22K0654, KME22K0691, KME22K0694, KME22K0715, KME22K0777, KME22M0921, KME23A0132, KME23A0714, KME23B1443

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 65 of 123

Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082085

Z-1891-2023
Recall number
Z-1891-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
39550 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341457, Batch Numbers: 18HG37, 18HT15, 18HT24, 18JG12, 18JG31, 19CT69, 19CT73, 19CT74, 19CT76, 19CT77, 19DT05, 19DT10, 19KT14, 19KT30, 19KT46, 19KT49, 19KT50, 19KT55, 19LT35, 20BT51, 20CT02, 20CT22, 20CT28, 20CT32, 20CT42, 20DT02, 20DT17, 20DT18, 20ET17, 20GG43, KME20H0750, KME20J2539, KME20J2680, KME20K0923, KME20K1114, KME20K1513, KME20K3034, KME20K3146, KME20L1867, KME20L2274, KME20M1511, KME21E0902, KME21F0741, KME21F1214, KME21F2006, KME21F2074, KME21K0095, KME21K1193, KME21K2275, KME21K2575, KME21K3015, KME21L0394, KME21L0799, KME21L1115, KME21L1276, KME21L1586, KME21M2500, KME21M2728, KME22A0787, KME22A2287, KME22A2957, KME22A2968, KME22B0519, KME22B1154, KME22B1696, KME22B1775, KME22B2179, KME22B2320, KME22B2477, KME22B2797, KME22C2074, KME22D1891, KME22D1892, KME22D3186, KME22D3488, KME22D3564, KME22E0663, KME22E0988, KME22E1279, KME22E1583, KME22E1811, KME22E2253

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 66 of 123

Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082090

Z-1892-2023
Recall number
Z-1892-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
30423 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341464, Batch Numbers: 18FG23, 18FT17, 18FT24, 18FT25, 18FT49, 18GG12, 18GG26, 18JG38, 18KG04, 18KG05, 18KG23, 18KG26, 18KG38, 18KT04, 18KT27, 18LG13, 19AT19, 19CG02, 19ET11, 19JT61, 19KT35, 19LT35, 19LT46, 20AT57, 20BT38, 20DT28, KME20H0415, KME20H2140, KME20H2314, KME20H2913, KME20J1999, KME20K0212, KME20K0600, KME20K1434, KME20K3525, KME20L0805, KME21K0478, KME21L1274, KME21L1371, KME22A2199, KME22A2286, KME22A2317, KME22B1140, KME22B1997, KME22B2180, KME22C0133, KME22C0202, KME22C0454, KME22C0573, KME22C0675, KME22D3492, KME22E1281, KME22E1282, KME22E2749, KME22F2444, KME22H2380, KME22K0996, KME23A2734, KME23B2546

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 67 of 123

Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082095

Z-1893-2023
Recall number
Z-1893-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
18620 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341471, Batch Numbers: 18HG08, 18HT04, 18IG29, 18IT04, 18JT16, 18KG37, 18KT27, 18LT16, 19BG02, 19CG02, 19CT04, 19CT72, 19GT25, 19HT19, 19HT47, 19JT05, 19KT55, 19LT08, 20AT13, 20CT02, 20CT29, 20DT32, 20GT23, 20GT44, KME20H1486, KME20J1899, KME20K2166, KME20L1592, KME20L2462, KME20L2557, KME20M2115, KME20M2198, KME21A2346, KME21E1393, KME21K1818, KME22B1259, KME22B1420, KME22B1854, KME22C0677, KME22C0713, KME22C0844, KME22C1612, KME22C2606, KME22C2757, KME22D1593, KME22D1778, KME22E1285, KME22E2362, KME22F1401, KME22F2452, KME23A0557, KME23A0763

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 68 of 123

Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082100

Z-1894-2023
Recall number
Z-1894-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
19250 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341488, Batch Numbers: 18GG13, 18JG24, 18JG36, 18JT06, 18KG10, 18LG06, 19AG36, 19CG02, 19GT16, 19GT59, 19IT33, 19JT56, 19KT14, 19KT49, 20AT01, 20AT22, 20BG18, 20DT18, 20DT19, 20ET17, KME20H2141, KME20K1809, KME20K2553, KME20L0335, KME20M1341, KME20M2113, KME21A2342, KME21A2668, KME21C0017, KME21F2252, KME21F2345, KME22B1777, KME22B1881, KME22C0019, KME22C0063, KME22C0327, KME22E2679, KME22F0401, KME22H0209, KME22H2251, KME22J2931, KME22J3329, KME22L0218, KME22L0219, KME22L2730, KME22L2731, KME23A2196, KME23A2539, KME23A3169

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 69 of 123

RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480025

Z-1895-2023
Recall number
Z-1895-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
66244 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341495, Batch Numbers: 18FG31, 18GT32, 18IG03, 18IG29, 18KG08, 18LG03, 19AG08, 19AG38, 19BG12, 19BG35, 19DT13, 19DT36, 19ET51, 19FT12, 19FT28, 19GT02, 19HT05, 19HT79, 19IT59, 19LT08, 19LT31, 20BG15, 20BT01, 20CT07, 20DT24, 20ET53, 20GT38, KME20H2416, KME20H2417, KME20J1068, KME20K2143, KME20K2598, KME20L0449, KME20L1346, KME20M0127, KME20M1797, KME21A0348, KME21B0087, KME21B0465, KME21C0163, KME21C1805, KME21C2447, KME21C2688, KME21C3244, KME21K2877, KME22A1408, KME22A2390, KME22A2545, KME22B0845, KME22B2017, KME22B2848, KME22C2802, KME22E0598, KME22E2130, KME22E2191, KME22G1878, KME22G2593, KME22H0532, KME22H1185, KME22H2178, KME22H2180, KME22J1309, KME22J2321

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 70 of 123

RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480030

Z-1896-2023
Recall number
Z-1896-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
21284 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341501, Batch Numbers: 18GG16, 18HG10, 18HG25, 18IG03, 19BG12, 19BG16, 19CT42, 19CT64, 19DT36, 19ET09, 19ET31, 19ET53, 19GT02, 19IT38, 19JT21, 19JT55, 19KT20, 19KT37, 19LT31, 20AT40, 20DT01, 20DT20, 20ET30, 20GT38, KME20J3096, KME20K2145, KME20L1345, KME20M1802, KME21B0621, KME21B2379, KME21C0168, KME22A1495, KME22A2394, KME22A2396, KME22B2938, KME22C2668, KME22C2669, KME22C2687, KME22D3223, KME22E1149, KME22E2287, KME22G1233, KME22G1879, KME23B0133, KME23B0560, KME23B0717, KME23B2197

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 71 of 123

RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480035

Z-1897-2023
Recall number
Z-1897-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
31945 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341518, Batch Numbers: 18GG15, 18GG16, 18IG01, 18IG03, 18IG04, 18IG13, 18LG30, 19BG16, 19BG35, 19DT35, 19ET51, 19GT51, 19IT38, 19JT20, 19JT50, 19KT37, 19KT60, 19LT03, 19LT27, 20AT54, 20BT42, 20BT51, 20CT07, 20CT54, 20ET30, 20FT43, KME20H2894, KME20J0754, KME20J3097, KME20M2591, KME20M3049, KME20M3050, KME21A0349, KME21A3147, KME21A3239, KME21B1099, KME21C1766, KME21C2690, KME21C3242, KME21D0295, KME21D2960, KME21K1922, KME21M0820, KME21M2050, KME21M3073, KME22A0416, KME22A1499, KME22B2850, KME22C1453, KME22C1455, KME22C2694, KME22D1761, KME22D2536, KME22E0601, KME22F2453, KME22G0614, KME22G1180, KME22G1181, KME22G1876, KME22H2913, KME22H3442, KME22J2322, KME22J3348, KME22L1190, KME22L1191, KME22L1547, KME23A2353, KME23A2534, KME23B0590, KME23C0083

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 72 of 123

RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480040

Z-1898-2023
Recall number
Z-1898-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
37076 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341525, Batch Numbers: 18FG14, 18FG22, 18JG08, 18KG25, 18LG04, 18LG30, 19DT35, 19DT36, 19ET09, 19ET31, 19ET51, 19HT60, 19IT32, 19IT43, 20AT06, 20AT39, 20BT01, 20BT53, 20CT12, 20CT27, 20CT54, 20DT04, 20ET30, 20FT58, KME20G0182, KME20H0372, KME20H0373, KME20J0924, KME20J2043, KME21C2368, KME21K1187, KME21K1188, KME21K1977, KME21M1084, KME21M1842, KME21M1845, KME21M2733, KME21M2734, KME21M2735, KME21M2736, KME22B2019, KME22C1693, KME22D0057, KME22D0180, KME22D0819, KME22D1066, KME22D3269, KME22E0602, KME22E2648, KME22E2681, KME22F1440, KME22F1692, KME22F2455, KME22G2312, KME22H1126, KME22H1212, KME22H2302, KME22J1615, KME22K0283, KME22K0632, KME22K1096, KME22M1155, KME22M1478, KME22M1659, KME23B3174

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 73 of 123

RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480045

Z-1899-2023
Recall number
Z-1899-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
30391 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341532, Batch Numbers: 18FG02, 18FG14, 18GT16, 18HG37, 18IG13, 18KG34, 18LG03, 19AG04, 19AG08, 19AG23, 19AG38, 19BG35, 19CG05, 19DT09, 19FT12, 19IT38, 19JT19, 19JT21, 19KT58, 19LT09, 19LT27, 20AT06, 20BG15, 20CT07, 20CT12, 20CT54, 20DT01, 20DT09, 20ET30, 20FT58, 20GT22, KME20H0774, KME20J0792, KME20J2687, KME20M0861, KME20M1576, KME20M1925, KME20M1926, KME20M3207, KME21A0769, KME21B0450, KME21C0314, KME21C1807, KME21K1189, KME21K1920, KME21M1895, KME21M2015, KME21M2776, KME21M3038, KME22B2939, KME22C0808, KME22C0928, KME22D0939, KME22D0940, KME22D1836, KME22D2309, KME22F0391, KME22F1537, KME22F2459, KME22F2526, KME22G1183, KME22H0051, KME22H3521, KME22J2886, KME22K1019, KME22M2104, KME23A1068, KME23A1487, KME23A2313

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 74 of 123

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150020

Z-1900-2023
Recall number
Z-1900-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
2550 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 4026704319640, Batch Numbers: 18FG01, 18FG05, 18HG07, 18HG22, 18HG27, 18HG38, 18IG02, 18JG04, 18JG06, 18JG17

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 75 of 123

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150025

Z-1901-2023
Recall number
Z-1901-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
2382 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 4026704319657, Batch Numbers: 18GT32, 18HG07, 18HG16, 18HG29, 18HG38, 18IG06, 18IG17, 18IG21, 18IG27

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 76 of 123

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150030

Z-1902-2023
Recall number
Z-1902-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
870 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 4026704319664, Batch Numbers: 18IG15, 18IG21, 18IG27, 18JG02, 18JG14

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 77 of 123

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150035

Z-1903-2023
Recall number
Z-1903-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
510 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 4026704319671, Batch Numbers: 18FG15, 18GG12, 18GG14, 18JG02

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 78 of 123

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150040

Z-1904-2023
Recall number
Z-1904-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
447 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 4026704319688, Batch Numbers: 18IG12, 18IG15

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 79 of 123

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150055

Z-1905-2023
Recall number
Z-1905-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
70 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 4026704319718, Batch Numbers: 18FG05

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 80 of 123

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181055

Z-1922-2023
Recall number
Z-1922-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
24752 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340573, Batch Numbers: 18FT35, 18GG18, 18GG23, 18GT32, 18IG16, 18JG35, 18KG01, 18KG39, 18LG15, 18LG18, 18LG39, 19AG01, 19AG25, 19CG02, 19CT33, 19DT05, 19DT35, 19ET36, 19ET61, 19ET65, 19KT02, 20AT26, 20CT11, 20DT19, KME21A2087, KME21B1774, KME21B2624, KME21B2710, KME21B2711, KME21C0549, KME22A0758, KME22A2298, KME22A2299, KME22B1465, KME22B1666, KME22B2680, KME22C2315, KME22C2316, KME22D1671, KME22D2352, KME22E1006, KME22E1007, KME22E1406, KME22E1930, KME22F2204, KME22F2482

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 81 of 123

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181060

Z-1923-2023
Recall number
Z-1923-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
8610 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340580, Batch Numbers: 18HG21, 18KG41, 18KG43, 18LG15, 19AG01, 19BG33, 19CT33, 19ET39, 19ET40, 19ET61, 19ET65, 20CT32, KME21M2381, KME22A2300, KME22C2820, KME22D1551, KME22D2353, KME22E1009, KME22E1144, KME22E1407, KME22F2205, KME22F3384

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 82 of 123

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181065

Z-1924-2023
Recall number
Z-1924-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
2980 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340597, Batch Numbers: 18FT35, 18GG25, 18JG35, 18KG21, 18LG18, 19AG25, 19CT33, 19ET69, 20BT02, 20CT11, KME22B1670, KME22E1010, KME22E1408, KME22H0137, KME22J0202, KME22K2262

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 83 of 123

Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380025

Z-1925-2023
Recall number
Z-1925-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
3590 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340610, Batch Numbers: 19ET51, 19FT29, 19GT05, 19GT35, 19HT79, 19JT51, 19KT06, 19LT28, 20AT05, 20AT37, 20AT54, 20BG15, 20DT24, 20ET03, KME21B0529, KME21C0887, KME21D0327, KME21F0137, KME21K0799, KME21K0800, KME22A2704, KME22C0981, KME22C1568, KME22D0029, KME22H0686, KME22H1360

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 84 of 123

Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380030

Z-1926-2023
Recall number
Z-1926-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
5990 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340627, Batch Numbers: 19ET31, 19FT28, 19GT08, 19GT31, 19GT35, 19GT48, 19HT05, 19HT32, 19HT60, 19IT38, 20DT09, 20DT24, 20ET03, 20FT55, 20GT37

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 85 of 123

Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380035

Z-1927-2023
Recall number
Z-1927-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
2860 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340634, Batch Numbers: 18HG08, 18IG13, 18JG35, 18LG31, 19BG15, 19CT16, 19ET31, 19HT07, 19HT79, 19LT28, 20GT37, KME20H2590, KME20L0690, KME22D0945, KME22E1145, KME22G2935, KME22J0819, KME22J2900

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 86 of 123

Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380040

Z-1928-2023
Recall number
Z-1928-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
3370 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340641, Batch Numbers: 19FT28, 19GT04, 19GT51, 19KT13, 19LT28, 20BG15, 20ET03, KME20H2609, KME20J3088, KME20K2749, KME20L0640, KME20M1726, KME20M2538, KME21A0858, KME21M2918, KME22B2857, KME22C3373, KME22D0876

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 87 of 123

Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380045

Z-1929-2023
Recall number
Z-1929-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
3031 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340658, Batch Numbers: 18FG22, 18GT16, 18IG04, 18JG08, 19CT42, 19HT05, 19HT61, 19JT51, 19KT13, 20DT04, KME20J0756, KME20K2144, KME20L0425, KME21A2196, KME21A3268, KME21C0914, KME22D0877, KME22E0896, KME22F1601, KME22G1456, KME22G2369

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 88 of 123

Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380050

Z-1930-2023
Recall number
Z-1930-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
4110 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340665, Batch Numbers: 18FG05, 18FT26, 18GT27, 18IG06, 18JG20, 18LG03, 18LT24, 19BG30, 19CT50, 19DT17, 19KT21, 19LT51, 20AT26, 20AT41, 20CT43, 20DT13, 20GG27, KME20H2359, KME20K1713, KME20L1811, KME20M2219, KME21A2253, KME21B0984, KME21L0988, KME22D2223, KME22D3339, KME22E0284, KME22F3118, KME22H2816

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 89 of 123

Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380055

Z-1931-2023
Recall number
Z-1931-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
1670 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340672, Batch Numbers: 19ET11, 19GT51, 19JT20, 20AT13, KME20H2315, KME21A2778, KME22A0155, KME22A2335, KME22E0288, KME22E1272, KME22F1551

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 90 of 123

Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380060

Z-1932-2023
Recall number
Z-1932-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
1110 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340689, Batch Numbers: 18FG31, 19BT11, 19ET72, 19JT30, 20AT13, 20BT13, 20DT13, KME21D0600, KME21J0790, KME22A0448, KME22D1803

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 91 of 123

Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380065

Z-1933-2023
Recall number
Z-1933-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
190 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340696, Batch Numbers: 19GT16, 19KT41, KME21D0517

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 92 of 123

Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382025

Z-1934-2023
Recall number
Z-1934-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
25630 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340788, Batch Numbers: 18FG22, 18FG31, 18FT13, 18GG16, 18GG34, 18GT12, 18HG08, 18IG13, 18IG14, 18JG09, 18JG14, 18JG35, 18KG08, 18LG15, 19AG04, 19AG07, 19AG21, 19BG12, 19CT37, 19CT41, 19CT44, 19CT64, 19ET57, 19FT25, 19GT04, 19GT29, 19KT65, 19LT03, 19LT27, 20AT37, 20BT15, 20CT12, 20DT04, 20ET03, 20ET33, 20FT21, 20FT40, 20GG41, KME20K2027, KME20K3208, KME21C1802, KME21C2684, KME21D0352, KME21D0601, KME21D1281, KME21D1818, KME21E1427, KME21M3077, KME22B1025, KME22B1089, KME22C0099, KME22E0297, KME22F0538, KME22F2559, KME22F2561, KME22G0176, KME22H1542, KME22K0062, KME22K0425, KME22K2437, KME22K2588, KME22L2985

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 93 of 123

Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382040

Z-1935-2023
Recall number
Z-1935-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
17102 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340818, Batch Numbers: 18FG31, 18FG33, 18FT13, 18GG15, 18HG08, 18HG10, 18HG25, 18IG13, 18JG08, 18KG09, 18KG33, 18LG01, 19BG12, 19BG35, 19ET09, 19FT12, 19GT05, 19IT11, 19KT20, 19KT38, 20AT37, 20CT12, 20CT53, 20DT04, 20ET56, 20FT21, 20FT43, 20GT18, KME20G0126, KME20H0286, KME20H1091, KME20H2041, KME20J2613, KME20K0326, KME20K0601, KME20M0209, KME20M1518, KME21B1133, KME21B1830, KME21C1573, KME21C1675, KME21C2245, KME21C3124, KME21D0525, KME21J0629, KME21K0797, KME21L2516, KME21L2526, KME21M0868, KME22C2637, KME22D0032, KME22D0811, KME22D0943, KME22D1009, KME22E0606, KME22E1274, KME22E2288

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 94 of 123

Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382045

Z-1936-2023
Recall number
Z-1936-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
11188 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340825, Batch Numbers: 18GG15, 18GG26, 18HG25, 18IG04, 18IG14, 18IG29, 18JG08, 18JG35, 18KG08, 18LG01, 19BG12, 19DT13, 19GT35, 19KT13, 19LT50, 20CT11, 20FT43, 20GT22, 20GT37, KME20H0783, KME20J2818, KME20J2819, KME20J2846, KME20K0469, KME20M1075, KME21B0085, KME21B1134, KME21B1828, KME21C1577, KME21C2244, KME21C2444, KME21D2950, KME21D2951, KME22D2158, KME22D2478, KME22E0295, KME22E0608, KME22E0909, KME22E0911, KME22E1313, KME22E2291, KME22J3174, KME22K2663, KME22K2686, KME22M0003, KME22M1623, KME23A2310, KME23B0782

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 95 of 123

Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382055

Z-1937-2023
Recall number
Z-1937-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
7800 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340849, Batch Numbers: 18FG21, 18FG33, 18FT17, 18FT31, 18GT06, 18HG06, 18HG15, 18IT06, 18JG14, 18JT12, 18KG10, 19AG05, 19AT23, 19BG10, 19BG21, 19BG26, 19BT08, 20CT47, 20DT01, 20GG45, 20GT40, KME20H0294, KME20H3036, KME20J0600, KME20J2166, KME20K1116, KME20K1206, KME20K3277, KME20L1040, KME20L1224, KME22F2548

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 96 of 123

Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382060

Z-1938-2023
Recall number
Z-1938-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
5600 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340856, Batch Numbers: 18FG02, 18FG28, 18FT08, 18FT33, 18JG15, 18KG23, 18KG39, 20BT17, 20CT07, KME20H1758, KME20H2730, KME21D0828, KME21J0120, KME21J1583, KME22A2339, KME22B0949, KME22B1778, KME22C2310, KME22D1804, KME22F0417, KME22F0556, KME22F1739

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 97 of 123

Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382065

Z-1939-2023
Recall number
Z-1939-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
2140 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704340863, Batch Numbers: 18KG25, 19BT19, 19CT22, 19CT39, 19ET06, KME21L2054, KME22A2341, KME22C2640, KME22E2541, KME22F1554, KME22F2582

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 98 of 123

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780035

Z-1940-2023
Recall number
Z-1940-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
36135 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341037, Batch Numbers: 18GG03, 18GG24, 18GT26, 18HG36, 18IG11, 18JG07, 18JG14, 18JG36, 18KG22, 18KG34, 18LG31, 19AG21, 19AG36, 19BG12, 19CG07, 19CT36, 19CT69, 19DT42, 19FT22, 19FT49, 19GT43, 19HT03, 19JT01, 19JT20, 19JT55, 19LT32, 20AT09, 20CT24, 20DT15, 20ET04, 20ET56, 20GG43, 20GT18, KME20H2627, KME20L2489, KME20M0355, KME20M1519, KME21A0965, KME21A2395, KME21B1964, KME21B2528, KME21C0337, KME22A1674, KME22B1172, KME22B1719, KME22C0647, KME22D0114, KME22D2229, KME22E0680, KME22E1094, KME22E2895, KME22E2896, KME22F1454, KME22F1458, KME22F2737, KME22G0575, KME22H0031, KME22H0797, KME22H1789, KME22H2875, KME22H3073, KME22J1158, KME22J1777, KME22K2438, KME22L1579, KME22L1617, KME22L1659, KME22L1725, KME23A2277, KME23A3144, KME23B0437

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 99 of 123

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780040

Z-1941-2023
Recall number
Z-1941-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
20042 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341044, Batch Numbers: 18FG24, 18GG03, 18GG04, 18GG24, 18GT26, 18HG24, 18JG07, 18KG22, 18KG34, 18LG33, 19AG36, 19BG12, 19CG07, 19CT69, 19DT42, 19ET58, 19FT18, 19GT43, 19GT44, 19JT55, 19KT38, 19LT32, 20AT09, 20AT49, 20BT53, 20DT24, 20ET50, 20FT36, 20FT60, 20GT40, KME21C0405, KME21C1057, KME22C0550, KME22C0648, KME22C1816, KME22C2806, KME22D1073, KME22D2150, KME22E0683, KME22E0684, KME22E2814, KME22E2897, KME22F1760, KME22F2739, KME22G0790, KME22H1304, KME22H2878, KME22J1447, KME22K0482, KME23A1241, KME23A2001, KME23A2181, KME23A2683, KME23A3032

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 100 of 123

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780045

Z-1942-2023
Recall number
Z-1942-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
23395 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341051, Batch Numbers: 18FG12, 18GG26, 18GT26, 18HG24, 18HG36, 18JG13, 18JG36, 18LG31, 18LG33, 19AG11, 19AG21, 19CG07, 19DT42, 19FT18, 19GT43, 19JT02, 19KT37, 19LT32, 20AT13, 20BT53, 20CT21, 20DT15, 20ET50, 20FT36, 20FT60, 20GG43, 20GT40, KME20K2722, KME20K2733, KME20L0659, KME20L1620, KME20M0897, KME20M1522, KME21A0198, KME21A0967, KME21A2397, KME21B2435, KME21C0325, KME22C1814, KME22C1815, KME22C2815, KME22D1075, KME22D3468, KME22E0686, KME22E2786, KME22F1459, KME22G0186, KME22G0338, KME22H1790, KME22J0267, KME22J1449, KME22J2193, KME22J2455, KME22K0574, KME22M1047, KME22M1305, KME22M1323, KME22M2819, KME22M3040, KME23A2332, KME23A2894, KME23A2895, KME23A3034

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 101 of 123

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780050

Z-1943-2023
Recall number
Z-1943-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
19842 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341068, Batch Numbers: 18FG12, 18FG24, 18GG03, 18GT26, 18HG24, 18IG24, 18JG07, 18KG34, 18LG11, 18LG31, 19AG09, 19AG11, 19AG21, 19AG36, 19CG07, 19CT36, 19DT06, 19FT18, 19GT44, 19JT01, 19KT37, 19LT04, 19LT32, 20AT09, 20BT53, 20CT24, 20DT24, 20ET50, 20ET56, 20FT36, 20FT58, KME20J1117, KME20M0952, KME21A0202, KME21A2486, KME21B0747, KME21C0326, KME22A1676, KME22B0553, KME22B1725, KME22C2818, KME22D0293, KME22D2681, KME22F0733, KME22G0349, KME22G3043, KME22H1792, KME22J2836, KME22K0470, KME22K0876, KME22M1319, KME22M1954, KME23A0157, KME23A1282, KME23A1422, KME23A1483, KME23A2002, KME23A2278, KME23B0506

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 102 of 123

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780055

Z-1944-2023
Recall number
Z-1944-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
14480 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341075, Batch Numbers: 18FG23, 18FG24, 18GG03, 18GT26, 18IT05, 18IT06, 18JG36, 18KG08, 18KG34, 18KG44, 18LG11, 18LG31, 19AG21, 19AG36, 19CT36, 19DT06, 19FT18, 19HT80, 19LT04, 20AT09, 20AT49, 20DT14, 20FT59, 20FT60, KME20H2632, KME20J1207, KME20K0629, KME20K2746, KME20L0661, KME20L1622, KME20M0351, KME21A0978, KME21A2488, KME21B1917, KME21C1735, KME21E1424, KME22C0548, KME22C0549, KME22D0160, KME22D0263, KME22E1097, KME22F1274, KME22G0791, KME22H0940, KME22H2230, KME22H2331, KME22H3266, KME22J2275, KME22J2875, KME22K2770, KME23A0296, KME23A0482, KME23A0601, KME23A2865, KME23A3176

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 103 of 123

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780060

Z-1945-2023
Recall number
Z-1945-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
16570 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341082, Batch Numbers: 18FG12, 18FG23, 18GG03, 18GT26, 18HG24, 18JG14, 18KG08, 18KG22, 18LG31, 19AG09, 19AG11, 19AG21, 19DT42, 19ET34, 19FT18, 19GT44, 19HT66, 19JT01, 19JT20, 19KT17, 19LT04, 19LT08, 19LT31, 19LT32, 20AT09, 20CT23, 20DT29, KME20L1712, KME20M0352

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 104 of 123

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780065

Z-1946-2023
Recall number
Z-1946-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
14780 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341099, Batch Numbers: 18FG12, 18FG23, 18FG24, 18GT26, 18HG24, 18IG11, 18IG14, 18IG24, 18JG07, 18JG36, 18KG10, 18LG11, 18LG31, 19AG11, 19AG36, 19CT36, 19DT10, 19ET12, 19FT18, 19FT49, 19HT03, 19HT66, 19IT43, 19JT20, 19KT21, 19LT08, 19LT31, 20AT49, 20BT53, 20DT14, 20DT24, 20FT59, KME20H0325, KME20J1141, KME20L0727, KME20M0906, KME20M2652, KME21B0072, KME21C0332, KME21C0923, KME21C3299, KME21D0466, KME21D1903, KME21L1006, KME21L1007, KME21M1776, KME21M3025, KME21M3026, KME22A0377, KME22B1011, KME22C1836, KME22C2817, KME22D1076, KME22D2087, KME22F1763, KME22G1315, KME22G3080, KME22H0004, KME22H2233, KME22J1231, KME22J2727, KME22K0999, KME22K1158, KME22K1240, KME22M3068

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 105 of 123

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780070

Z-1947-2023
Recall number
Z-1947-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
25520 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341105, Batch Numbers: 18FG12, 18FG24, 18GG01, 18GG26, 18GT26, 18HG36, 18IG14, 18IT05, 18JG07, 18KG10, 18KG34, 18LG11, 18LG31, 19AG36, 19CG07, 19CT69, 19ET12, 19GT39, 19GT44, 19HT80, 19IT12, 19IT43, 19JT01, 19JT55, 19KT21, 19LT08, 19LT31, 20AT13, 20AT49, 20BT53, 20CT24, 20DT09, 20DT24, 20ET50, 20FT39, 20FT59, 20GG27, KME20J2813, KME20J3155, KME20K1111, KME20K2068, KME20K3244, KME20L0730, KME20L0731, KME20L1681, KME20M0276, KME20M0955, KME20M2655, KME21A0979, KME21B0096, KME21B0154, KME21B1518, KME21C0334, KME21M1046, KME22A0450, KME22A1594, KME22B0425, KME22B1002, KME22C0473, KME22D1110, KME22D2351, KME22D2363, KME22D3366, KME22D3379, KME22E1102, KME22E2443, KME22F1333, KME22G0171, KME22G1728, KME22G3156, KME22H0815, KME22H1321, KME22J0749, KME22K1286, KME22K2440, KME22L1550, KME22L1660, KME22L2544

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 106 of 123

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780080

Z-1948-2023
Recall number
Z-1948-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
9070 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341129, Batch Numbers: 18FG33, 18GG23, 18GG34, 18HG30, 18IG11, 18IG18, 18JG21, 18JG35, 18KG19, 18KG41, 19AG15, 19BG04, 19BG19, 19GT65, 19HT68, 19IT15, 19LT21, 20AT26, 20CT12, 20CT13, 20CT32, 20DT35, 20FT19, KME20M3089, KME20M3090, KME21A1299, KME21A2090, KME21B0716, KME21B1783, KME21B1962, KME21B2204, KME21B2676, KME21C0599, KME22B0591, KME22C2317, KME22D0156, KME22D2122, KME22D2752, KME22E1153, KME22G0816, KME22H2094, KME22H2235, KME22H3271, KME22J0148, KME22J0532, KME22J3210, KME22K2844

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 107 of 123

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780085

Z-1949-2023
Recall number
Z-1949-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
670 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341136, Batch Numbers: 18GG25, 18LG18, 19AG19, 19DT36, 20CT32, 20GT34, KME21B2675, KME21F0887, KME22H1797

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 108 of 123

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780090

Z-1950-2023
Recall number
Z-1950-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
200 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341143, Batch Numbers: 18HG23, 19BG19, 19CT36

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 109 of 123

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781035

Z-1951-2023
Recall number
Z-1951-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
76060 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/I 14026704341150, Batch Numbers: 18FG20, 18FG31, 18GG23, 18GG34, 18GT32, 18HG17, 18IG15, 18JG01, 18JG16, 18JG35, 18KG17, 18KG18, 18KG36, 18LG15, 18LG30, 18LG39, 19AG15, 19BG33, 19CG01, 19CG02, 19CT26, 19DT03, 19DT30, 19DT38, 19ET58, 19ET69, 19FT37, 19FT46, 19IT53, 19JT10, 19KT14, 19KT46, 19LT16, 20AT22, 20AT26, 20CT11, 20CT32, 20DT19, 20DT32, 20ET34, 20ET49, 20FT18, 20FT64, 20GT11, KME20H0466, KME20H2769, KME20H2998, KME20H3129, KME20M0650, KME20M1283, KME20M2799, KME20M2822, KME21A2028, KME21A3020, KME21B1044, KME21B1197, KME21B1960, KME21B1961, KME21C0324, KME21C0426, KME21C1119, KME21L0024, KME21L0026, KME21L1782, KME21L2301, KME21L2785, KME21M1710, KME21M2600, KME21M2601, KME22A0560, KME22A0755, KME22A1376, KME22C0493, KME22D1697, KME22D2626, KME22D2999, KME22D3173, KME22D3253, KME22E0727, KME22E0728, KME22E1011, KME22E1155, KME22E1392, KME22E2151, KME22E2239, KME22E2744, KME22E2753, KME22F0075, KME22F0229, KME22F0540, KME22F0600, KME22F0880, KME22F1315, KME22F1736, KME22F2068, KME22F2353, KME22F2627, KME22F2949, KME22F3119, KME22F3242, KME22F3425, KME22G0214, KME22G0600, KME22G0898, KME22G1642, KME22G1861, KME22G2270, KME22G3150, KME22G3268, KME22H2027, KME22H3065, KME22H3272, KME22H3273, KME22H3400, KME22J0633, KME22J0901

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 110 of 123

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781050

Z-1952-2023
Recall number
Z-1952-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
302652 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341181, Batch Numbers: 18FG31, 18FT35, 18FT39, 18GG17, 18GG18, 18GT32, 18HG17, 18HG19, 18HG21, 18HG22, 18HG29, 18IG15, 18IG17, 18IG30, 18JG16, 18JG19, 18JG35, 18JG37, 18KG17, 18KG39, 18KG40, 18LG14, 18LG15, 18LG18, 18LG39, 19AG25, 19BG02, 19BG04, 19BG18, 19BG19, 19BG32, 19CG01, 19CT28, 19CT33, 19CT36, 19CT56, 19CT57, 19CT80, 19DT05, 19DT30, 19ET34, 19ET36, 19ET39, 19ET40, 19ET61, 19ET65, 19FT01, 19FT45, 19GT13, 19GT63, 19HT24, 19HT31, 19HT53, 19IT54, 19JT06, 19JT10, 19JT11, 19JT14, 19JT35, 19JT63, 19KT14, 19KT38, 19KT41, 19KT46, 19LT17, 19LT21, 20AT22, 20BT53, 20CT07, 20CT12, 20CT14, 20CT32, 20DT18, 20DT29, 20ET34, 20ET38, 20ET49, 20FT17, 20FT19, 20FT21, 20FT64, 20GT11, KME20J0370, KME20J0663, KME20J0665, KME20J1212, KME20K3628, KME20L2213, KME20L2286, KME20L2666, KME20L2668, KME20M0644, KME20M1284, KME20M2643, KME20M2645, KME20M2956, KME20M3015, KME21A1024, KME21A1065, KME21A1273, KME21A2079, KME21A2235, KME21A3066, KME21B0255, KME21B0256, KME21B0378, KME21B2209, KME21B2274, KME21B2275, KME21B2535, KME21C0433, KME21C0643, KME21C1123, KME21C1125, KME21C1164, KME21E0006, KME21F0902, KME21F1216, KME21F2139, KME21F2198, KME21J0892, KME21J1496, KME21J1690, KME21J1813, KME21J2074, KME21K0004, KME21K0115, KME21K0296, KME21K0875, KME21K0877, KME21K1029, KME21K1079, KME21K1716, KME21K1826, KME21K1868, KME21K2303, KME21K2335, KME21K3007, KME21L0889, KME21L0985, KME21L1526, KME21L1597, KME21L1776, KME21L2153, KME21L2154, KME21L2299, KME21L2885, KME21M0162, KME21M0337, KME21M0342, KME21M0502, KME21M0733, KME21M0951, KME21M1978, KME21M1979, KME21M2427, KME21M2675, KME21M2676, KME21M2711, KME21M2807, KME22A0564, KME22A0565, KME22A1888, KME22A2257, KME22A2369, KME22A2370, KME22A2850, KME22A2919, KME22A2970, KME22B0006, KME22B0174, KME22B0360, KME22B0400, KME22B0665, KME22B0754, KME22B2315, KME22B2554, KME22B2557, KME22B2631, KME22B2633, KME22B2635, KME22B2678, KME22B2793, KME22B2794, KME22B2920, KME22C0553, KME22C1122, KME22C3230, KME22C3394, KME22C3396, KME22D0097, KME22D0108, KME22D0244, KME22D0286, KME22D0322, KME22D0538, KME22D0539, KME22D0602, KME22D0805, KME22D0854, KME22D0936, KME22D1008, KME22D1453, KME22D1957, KME22D2058, KME22D2293, KME22D2643, KME22D2765, KME22D3013, KME22E0947, KME22E0956, KME22E1500, KME22E1885, KME22E2219, KME22E2220, KME22E2440, KME22E2512, KME22E2872, KME22F0074, KME22F0542, KME22F0987, KME22F1112, KME22F2173, KME22F2206

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 111 of 123

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781055

Z-1953-2023
Recall number
Z-1953-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
172721 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341198, Batch Numbers: 18FT35, 18FT39, 18GG17, 18GG18, 18GT32, 18IG10, 18IG16, 18IG17, 18JG13, 18JG20, 18JG35, 18JG37, 18KG18, 18KG39, 18KG41, 18LG12, 18LG14, 18LG30, 18LG39, 19AG29, 19BG03, 19BG04, 19BG18, 19BG19, 19BG33, 19CG01, 19CG02, 19CG04, 19CT28, 19CT33, 19CT56, 19DT03, 19DT30, 19DT35, 19DT42, 19DT46, 19ET16, 19ET34, 19FT01, 19GT63, 19HT31, 19HT55, 19IT01, 19IT12, 19IT14, 19IT15, 19IT19, 19KT02, 19KT41, 19LT17, 20BT01, 20BT02, 20CT07, 20DT18, 20DT29, 20DT32, 20ET34, 20ET49, 20FT18, 20FT64, 20GT11, 20GT34, 20GT49, KME20H0487, KME20H1788, KME20H2574, KME20H2768, KME20H3002, KME20J1213, KME20L0905, KME20L2170, KME20L2191, KME20L2670, KME20M0304, KME20M2647, KME20M3094, KME21A1082, KME21A2080, KME21A2926, KME21B0543, KME21B1199, KME21B1630, KME21B1716, KME21B2541, KME21B2670, KME21C0592, KME21C0593, KME21C3340, KME21D2002, KME21E0008, KME21E0009, KME21F0901, KME21F1424, KME21F1459, KME21F2371, KME21J1239, KME21J1487, KME21J1691, KME21J1692, KME21J1854, KME21K0178, KME21K1046, KME21K1078, KME21K2304, KME21K3005, KME21L0631, KME21L0756, KME21L1428, KME21L1429, KME21L1596, KME21L2141, KME21L2291, KME21L2736, KME22A1889, KME22A1890, KME22A2018, KME22A2281, KME22A2921, KME22A2969, KME22B0359, KME22C0207, KME22C2843, KME22C2927, KME22C2969, KME22C3213, KME22C3304, KME22C3375, KME22C3379, KME22D0052, KME22D0587, KME22D0719, KME22D0808, KME22D0844, KME22D0846, KME22D0855, KME22D0899, KME22D1001, KME22D1093, KME22D1115, KME22D1337, KME22D1348, KME22D1454, KME22D1568, KME22D1675, KME22D1820, KME22D2489, KME22D2490, KME22D3014, KME22D3071, KME22E1106, KME22E1398, KME22E1402, KME22E1502, KME22E1580, KME22E1581, KME22E1629, KME22E1778, KME22E1851, KME22E1931, KME22E2306, KME22F0073, KME22F0543, KME22F1077, KME22G1333, KME22G2578, KME22H1508, KME22H2499, KME22H3402, KME22K0250

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 112 of 123

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781060

Z-1954-2023
Recall number
Z-1954-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
43571 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341204, Batch Numbers: 18FT39, 18GT32, 18HG19, 18IG10, 18IG16, 18IG30, 18JG35, 18LG15, 18LG30, 19AG15, 19AG25, 19CT33, 19CT36, 19DT35, 19DT46, 19ET34, 19ET69, 19FT01, 19GT13, 19GT17, 19GT63, 19HT68, 19IT01, 19IT53, 19JT15, 19JT35, 19KT41, 19LT21, 19LT36, 20AT22, 20BT02, 20CT32, 20DT35, 20ET34, 20ET39, 20FT18, 20FT64, KME20H0431, KME20L2192, KME20M0306, KME20M1285, KME20M2828, KME20M2905, KME21A1085, KME21A2932, KME21A3056, KME21B0722, KME21B1047, KME21B1628, KME21B2706, KME21C1054, KME21C2465, KME21C3344, KME21D2006, KME21D2007, KME21F1423, KME21J1549, KME21K3004, KME21L1432, KME21L2739, KME21M0028, KME21M0163, KME21M0799, KME21M2429, KME21M2911, KME21M3080, KME22A0809, KME22A1219, KME22B1419, KME22C1123, KME22C1555, KME22C1556, KME22C2192, KME22C2845, KME22C2970, KME22D0540, KME22D1570, KME22D1620, KME22D1841, KME22D2294, KME22D2491, KME22E2435, KME22E2436, KME22E2874, KME22G0208, KME22G0690, KME22G0862, KME22G1268, KME22G2247, KME22G2660, KME22G3252, KME22H1630, KME22H2409, KME22J1083, KME22J2876

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 113 of 123

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781065

Z-1955-2023
Recall number
Z-1955-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
37890 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341211, Batch Numbers: 18FG20, 18FG31, 18GG17, 18HG21, 18IG16, 18IG30, 18JG16, 18JG20, 18KG01, 18LG30, 19AG01, 19AG25, 19AG29, 19BG18, 19CG02, 19DT35, 19DT46, 19ET36, 19FT01, 19FT02, 19FT45, 19GT63, 19HT55, 19HT68, 19IT53, 19KT14, 19KT46, 19LT17, 19LT21, 20AT22, 20BT01, 20CT11, 20CT32, 20DT19, 20ET39, 20FT18, 20FT64, KME20H0432, KME20H2681, KME20L2673, KME20M1288, KME20M2831, KME20M2957, KME21A2081, KME21A2935, KME21B0719, KME21B1201, KME21B1825, KME21B1947, KME21C0646, KME21C1045, KME21C3350, KME21D1229, KME21E0011, KME21F0146, KME21K1657, KME21K1658, KME21K1713, KME21K1748, KME21L2302, KME21L2792, KME21L2886, KME22A1379, KME22A1884, KME22A1885, KME22A2922, KME22C0332, KME22C0413, KME22C1125, KME22C1127, KME22C1581, KME22C2971, KME22D0261, KME22D1843, KME22D3133, KME22E0948, KME22E0949, KME22F0366, KME22F0988, KME22F3121, KME22G0692, KME22G1335, KME22G3063, KME22H0521, KME22H1633, KME22H3274, KME22J0144, KME22J1123, KME22J2413, KME22J2479, KME22K0090

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 114 of 123

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781070

Z-1956-2023
Recall number
Z-1956-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
35513 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341228, Batch Numbers: 18GG17, 18GG25, 18GT32, 18HG19, 18IG16, 18JG13, 18JG21, 18KG01, 18LG12, 18LG15, 18LG30, 19AG15, 19AG25, 19AG29, 19BG03, 19CT56, 19GT17, 19HT02, 19HT31, 19HT68, 19HT69, 19IT19, 19JT11, 19JT35, 19KT02, 19LT21, 20AT22, 20BG11, 20CT11, 20DT22, 20DT35, 20FT64, 20FT68, 20GT34, 20GT49, KME20H0436, KME20H2683, KME20M0445, KME20M2650, KME21A2042, KME21A2083, KME21A2187, KME21A2929, KME21B0718, KME21B1715, KME21B1946, KME21C0552, KME21C1043, KME21C1044, KME21C1910, KME21C1912, KME21F1682, KME21F1864, KME21K1635, KME21M0798, KME21M2432, KME22A0810, KME22A2177, KME22A2883, KME22A2924, KME22A3263, KME22B2796, KME22C0042, KME22C0206, KME22C0505, KME22D2264, KME22D3154, KME22E1996, KME22E2224, KME22E2513, KME22F0202, KME22H0792, KME22H1588, KME22H2923, KME22J1124, KME22J2482, KME22J3020

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 115 of 123

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781080

Z-1957-2023
Recall number
Z-1957-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
8620 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341242, Batch Numbers: 18GG18, 18HG21, 18IG16, 18KG01, 18KG19, 18LG18, 19BG18, 19BG33, 19GT13, 19HT31, 19HT55, 19IT15, 19JT35, 19KT14, 19LT21, 20AT26, 20CT11, 20FT68, 20GT49, KME20M0409, KME21A1111, KME21A2095, KME21B2212, KME21C2483, KME21C3405, KME22B0921, KME22B0923, KME22D0289, KME22D1811, KME22D1855, KME22D2401, KME22E2898, KME22H2600, KME22H3295, KME22J2877, KME22K2861, KME22K3117, KME22M1510, KME22M2546, KME23B0521, KME23B3047

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 116 of 123

Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080050

Z-1958-2023
Recall number
Z-1958-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
1750 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341266, Batch Numbers: 18FG07, 18JG33, 18JG36, 18LT16, 19CT26, 19KT38, 19LT07, 20AT41, 20CT13, 20ET17, KME20K1512, KME22B0593, KME22E2347, KME22H1178, KME22H3021

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 117 of 123

Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080060

Z-1959-2023
Recall number
Z-1959-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
4160 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341266, Batch Numbers: 18GG26, 18GT08, 18GT11, 18IG22, 18IT18, 18JG33, 19AG39, 19ET31, 19GT25, 19IT20, 19KT14, 19KT47, 20AT58, 20CT13, 20FT66, KME20J1463, KME21K0521, KME22A2893, KME22B2215, KME22C2044, KME22G2998, KME22J0859

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 118 of 123

Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080065

Z-1960-2023
Recall number
Z-1960-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
6710 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341266, Batch Numbers: 18GT07, 18HG20, 18IG16, 18IG22, 18JG13, 19AT23, 19CT64, 19ET12, 19ET31, 19HT69, 19LT47, 20AT41, 20BT13, 20DT40, 20GT05, KME22A2193, KME22A2546, KME22B2739, KME22C2271, KME22E0189

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 119 of 123

Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080070

Z-1961-2023
Recall number
Z-1961-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
17950 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341266, Batch Numbers: 18FG19, 18GG19, 18HG28, 18IG06, 18IG19, 18JG13, 18JG17, 18KG13, 18LT07, 19BG19, 19CT26, 19DT20, 19ET12, 19ET36, 19HT26, 19HT69, 19JT21, 19KT14, 19LT31, 19LT51, 20AT22, 20AT58, 20BT13, 20BT42, 20CT13, 20DT10, 20ET12, 20FT11, 20FT19, 20GG40, 20GT38, KME20K2577, KME20L1985, KME20M1771, KME20M1772, KME21F1585, KME21J0644, KME21J1078, KME22A1109, KME22A1781, KME22B0401, KME22F1174, KME22F2171, KME22G1295, KME22G2999

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 120 of 123

Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080075

Z-1962-2023
Recall number
Z-1962-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
13810 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI Batch Numbers: 18FT26, 18GG17, 18GG19, 18HG15, 18HG37, 18IG04, 18IG29, 18JG17, 18KG10, 19AT23, 19CT64, 19ET12, 19ET24, 19GT31, 19HT69, 19IT11, 20AT22, 20BT13, 20BT42, 20CT02, 20CT54, 20DT09, 20FT21, 20FT60, 20GT18, KME20H0334, KME21F1534, KME22A2269, KME22B0741, KME22B0896, KME22B1031, KME22C0096, KME22E2348, KME22F2118,

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 121 of 123

Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080080

Z-1963-2023
Recall number
Z-1963-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
3843 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341266, Batch Numbers: 18FG02, 18GG15, 18IG13, 18IG22, 18JG17, 18JG38, 19BG21, 19DT19, 19GT24, 19HT26, 19JT20, 19KT19, 19KT38, 19KT50, 19LT46, 19LT47, 20AT06, 20BT09, 20DT23, 20GG39, KME21G0866, KME22A2268, KME22B0062

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 122 of 123

Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080085

Z-1964-2023
Recall number
Z-1964-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
1280 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341266, Batch Numbers: 18IG19, 18KG26, 19CT61, 19GT31, 19JT19, 19KT38, 19LT17, 20CT02, 20DT23, 20ET17, 20GT57, KME22A1989

Distribution pattern

US Nationwide distribution including Puerto Rico.

device · product 123 of 123

Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080090

Z-1965-2023
Recall number
Z-1965-2023
Initiated
May 25, 2023
Classification
Class I
Status
Ongoing
Recalling firm
TELEFLEX LLC
Quantity
670 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information

UDI/DI 14026704341266, Batch Numbers: 18FT24, 18FT26, 19ET83, 19GT29, 19KT58, 19KT38

Distribution pattern

US Nationwide distribution including Puerto Rico.