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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 77081

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

Open FDA event record

Event summary

Timeline bucket
April 21, 2017
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Teleflex Medical

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

4 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 4

PE CONNECTOR 3/8 STRAIGHT 20/BX, Sterile, Single use, Product Usage: Catheter Connector/Accessory

Z-2127-2017
Recall number
Z-2127-2017
Initiated
April 21, 2017
Classification
Class II
Status
Terminated
Recalling firm
Teleflex Medical
Quantity
19,043 units in total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Labeling: The expiration date is not stated on the labeling, there is a potential for expired product to be used.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling False and Misleading

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Labeling: The expiration date is not stated on the labeling, there is a potential for expired product to be used.

Code information

Product Code: PE100, Lot numbers: 02F0801115, 02F0901859, 02G0802748, 02G0900814, 02H0900192, 02K0900567, 02L0900163, 02M0901006, 74A1601695, 74G1500137, 74G1502714 & 74M1400489.

Distribution pattern

Worldwide Distribution - U.S. Nationwide. Foreign consignees: Australia, Canada, China, Columbia, India, San Salvador, Singapore and South Korea.

device · product 2 of 4

PE CONNECTOR 3/8 Y 20/BX, Sterile, Single use, Product Usage: Catheter Connector/Accessory

Z-2128-2017
Recall number
Z-2128-2017
Initiated
April 21, 2017
Classification
Class II
Status
Terminated
Recalling firm
Teleflex Medical
Quantity
19,043 units in total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Labeling: The expiration date is not stated on the labeling, there is a potential for expired product to be used.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling False and Misleading

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Labeling: The expiration date is not stated on the labeling, there is a potential for expired product to be used.

Code information

Product Code: PE101, Lot numbers: 02A1100078, 02A1403418, 02B0900484, 02B1201332, 02C1002327, 02C1101252, 02D0802669, 02D0803967, 02D1101333, 02D1101975, 02D1201492, 02E0900909, 02F0800279, 02F1101765, 02G0802046, 02G0900106, 02G0902858, 02G1302277, 02H0901652, 02H0902603, 02H1103939, 02K0900568, 02K1000269, 02K1001997, 02K1103123, 02K1301033, 02L0701464, 02L0901521, 02L1002578, 02L1003527, 74A1601696, 74C1601057, 74E1600942, 74E1602825, 74F1401270, 74H1501378, 74J1502624 & 74L1500554.

Distribution pattern

Worldwide Distribution - U.S. Nationwide. Foreign consignees: Australia, Canada, China, Columbia, India, San Salvador, Singapore and South Korea.

device · product 3 of 4

PE CONNECTOR 5 IN 1 20/BX, Sterile, Single use, Product Usage: Catheter Connector/Accessory

Z-2129-2017
Recall number
Z-2129-2017
Initiated
April 21, 2017
Classification
Class II
Status
Terminated
Recalling firm
Teleflex Medical
Quantity
19,043 units in total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Labeling: The expiration date is not stated on the labeling, there is a potential for expired product to be used.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling False and Misleading

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Labeling: The expiration date is not stated on the labeling, there is a potential for expired product to be used.

Code information

Product Code: PE102, Lot numbers: 02A1101041, 02B1102552, 02C1001258, 02C1003795, 02C1101253, 02C1104114, 02D0802670, 02D0803968, 02D1000682, 02D1002136, 02D1101334, 02E1001502, 02E1100384, 02F0800281, 02F1000667, 02F1002368, 02F1101766, 02F1102607, 02F1103754, 02G1000322, 02G1001538, 02H0801670, 02H0803375, 02H1000732, 02H1103023, 02H1103940, 02J1000236, 02J1001515, 02J1002609, 02J1003237, 02J1101139, 02J1102143, 02K1000270, 02K1001993, 02K1100519,02K1103124, 02K1301613, 02L0701463, 02L0701958, 02L0702675, 02L1000763, 02M0700783, 02M1001319, 74A1600225, 74A1600226, 74B1601947, 74B1601948, 74D1600917, 74F1401859, 74F1502294, 74F1502573, 74F1602371, 74H1601152, 74J1601641, 74K1501590 & 74L1500555.

Distribution pattern

Worldwide Distribution - U.S. Nationwide. Foreign consignees: Australia, Canada, China, Columbia, India, San Salvador, Singapore and South Korea.

device · product 4 of 4

INFANT 20/BX, Sterile, Single use Product Usage: Catheter Connector/Accessory

Z-2130-2017
Recall number
Z-2130-2017
Initiated
April 21, 2017
Classification
Class II
Status
Terminated
Recalling firm
Teleflex Medical
Quantity
19,043 units in total

App-derived interpretation

No assignment exists because the official recall reason is blank.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling False and Misleading

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Unavailable

Code information

Product Code: PE103, Lot numbers: 02B1300991, 02B1402029, 02C1301654, 02E1201155, 02H1302224, 02K1100520, 02K1103125, 02K1200732, 02K1202185, 02L0701465, 02L0701959, 02L1201668, 02L1203112, 02M1201149, 74A1601005 & 74F1400876.74H1601152, 74J1601641, 74K1501590 & 74L1500555.

Distribution pattern

Worldwide Distribution - U.S. Nationwide. Foreign consignees: Australia, Canada, China, Columbia, India, San Salvador, Singapore and South Korea.