Recall events
/
Event 79329
Event summary
Timeline bucket October 23, 2017
Product types Device
Classifications Class II
Statuses Terminated
Recalling firm wording Centurion Medical Products Corporation
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
21 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 21
SKIN STAPLE REMOVER
Z-1078-2018
Recall number Z-1078-2018
Initiated October 23, 2017
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1078-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[27602]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
Code information 44105 Lot codes: 2015083101 2016101701 2017082801 2017030601 2016072501
Distribution pattern Nationally
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[25947]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 21
SUTURE REMOVAL TRAY, SET or KIT
Z-1079-2018
Recall number Z-1079-2018
Initiated October 23, 2017
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1079-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[56353]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
Code information 55160 55395 55525 60125 60255 60360 60365 75435 84105 86125 SR530 Lot codes: 2016011801 2016011290 2016022390 2016042990 2016061390 2016080390 2016101790 2017011090 2015111990 2017022790 2015062201 2015081001 2016032101 2016050901 2016091201 2017032001 2017061501 2015042701 2015100501 2015120701 2016011101 2016071101 2016103101 2017011601 2017071201 2015100501 2016012501 2016071101 2016090501 2017013101 2017021601 2017051101 2017080701 2016060601 2017071101 2015111601 2016030701 2016101001 2015062201 2015110201 2016022201 2016091201 2015050401 2015082401 2016010401 2016072501 2017042401 2016101001 2017021301 2017071101 2016050201 2016111401 2015062901 2015081701 2015090701 2015110201 2016021501 2016040401 2016071101 2016102401 2016121401 2017021301 2017041901 2017070501 2017071801 2015072001 2016111401 2016021501 2016062001 2016081501 2016062701 2016040790 2015102990 2015120790 2016011890 2016050990 2016072590 2016091990 2017010390 2017012390 2017052290 2017062290 2015061501 2015081001 2015102601 2015122801 2016030701 2016050901 2016072501 2016101001 2016122701 2017041201 2017071001 2015060801 2015072001 2015082401 2015102601 2015122801 2016022201 2016050201 2016072501 2016091201 2016110701 2017022801 2017053101 2017060501 2016122001 2017041101
Distribution pattern Nationally
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[27065]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 21
GENERAL PURPOSE INSTRUMENT TRAY
Z-1080-2018
Recall number Z-1080-2018
Initiated October 23, 2017
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1080-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[38572]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
Code information 75121 75175 71435 75455 75690 SR245 Lot codes: 2017071990 2016110990 2016040790 2017022090 2016112490 2017010390 2017082390 2015101290 2015111790 2016032290 2016051790 2016053090 2016102490 2017013190 2017032990 2017080290 2015110390 2016010490 2016012090 2016020890 2016041890 2016061390 2016090590 2016110790 2017010990 2017021390 2017032190 2015092190 2015120190 2015121490 2016022590 2016120190 2017010390 2017011090 2015093090 2015112390 2016020390 2016092290 2016091590
Distribution pattern Nationally
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[21804]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 21
MINI PLASTICS SET
Z-1081-2018
Recall number Z-1081-2018
Initiated October 23, 2017
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1081-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[10807]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
Code information 75700 Lot codes: 2015102790 2016011590 2016030790 2016050490 2016062390 2016071590 2016081790 2016111890 2017012090 2017020790 2017042090
Distribution pattern Nationally
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[26546]
FDA event record
· Exact recall-number query on openFDA
device · product 5 of 21
CIRCUMCISION TRAY
Z-1082-2018
Recall number Z-1082-2018
Initiated October 23, 2017
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1082-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[56359]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
Code information CIT6020 CIT6120 Lot codes: 2015081790 2015112090 2016011190 2016022390 2016031690 2016042690 2016061590 2016080890 2016090690 2016100790 2017010990 2017020990 2017040490 2017051590 2017061690 2015111390 2016012190 2016022390 2016033190 2016060690 2016071890 2016092290 2016111590 2017020990 2017030790 2017041390 2017051590
Distribution pattern Nationally
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[26300]
FDA event record
· Exact recall-number query on openFDA
device · product 6 of 21
CATHETER SECUREMENT SYSTEM
Z-1083-2018
Recall number Z-1083-2018
Initiated October 23, 2017
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1083-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[15096]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
Code information CSS490 Lot codes: 2016022290 2017071790
Distribution pattern Nationally
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[27201]
FDA event record
· Exact recall-number query on openFDA
device · product 7 of 21
ST. CHRISTOPHER'S SECUREMENT SET
Z-1084-2018
Recall number Z-1084-2018
Initiated October 23, 2017
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1084-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[51367]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
Code information CSS685 Lot codes: 2015080390 2015092890 2015113090 2016011890 2016031490 2016042590 2016061390 2016071190 2016082290 2016092690 2016110790 2017011690 2017021390 2017031390 2017032790 2017081890
Distribution pattern Nationally
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[21844]
FDA event record
· Exact recall-number query on openFDA
device · product 8 of 21
SorbaView Shield Dressing Change Tray
Z-1085-2018
Recall number Z-1085-2018
Initiated October 23, 2017
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1085-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[34608]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
Code information DT12165 Lot codes: 2017050890 2016080290
Distribution pattern Nationally
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[26278]
FDA event record
· Exact recall-number query on openFDA
device · product 9 of 21
TUBING CHANGE KIT
Z-1086-2018
Recall number Z-1086-2018
Initiated October 23, 2017
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1086-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[56365]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
Code information DT6870 Lot codes: 2015110290 2016090890 2017042690
Distribution pattern Nationally
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[21831]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1087-2018
Initiated October 23, 2017
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1087-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[27606]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
Code information DT875 Lot codes: 2015102090 2015120290 2016012190 2016032290 2016052690 2016072890 2016090590 2017010490 2017020790 2017032190 2017042790
Distribution pattern Nationally
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[27229]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1088-2018
Initiated October 23, 2017
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1088-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[27601]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
Code information ID1090 ID1485 ID1525 ID1595 ID510 ID525 ID580 ID600 ID800 ID875 ID975 Lot codes: 2015102190 2016010790 2016020890 2016022390 2016061090 2016071990 2016101290 2016110390 2017011990 2016121690 2017022390 2017052690 2015101490 2016060690 2016070890 2016102490 2017032190 2017052390 2015091790 2015111990 2015112590 2016070890 2016072790 2016082390 2017020290 2017032890 2017052690 2017030390 2015092490 2015121490 2016010690 2016033190 2016042790 2016052490 2016061390 2016102790 2016112490 2017042890 2017063090 2017071990 2015100890 2017072890 2017040690 2016092290 2016031790 2016012190 2017030290 2016021890 2016060890 2016070790 2016080590 2016111190 2017010990 2017051190 2015110590 2015103090 2016071490 2015121590 2016031590 2016042090 2016051890 2016052590 2016062190 2016110190 2017010390 2017020890 2017040490 2017060890 2017062890 2017082290 2016112290 2016042790 2017060890 2017070790 2017082490 2015101590 2016022590 2016072890 2016090290 2017011190 2017040690 2017061690 2017081190 2017011690 2015092490 2015100890 2015111990 2016040690 2016060890 2016071890 2017013090 2016030790 2016031590 2016080190 2017010390 2017050490 2016072090 2015081190 2015102790 2016010490 2016022490 2016031190 2016060690 2016082990 2016111790 2017011790 2017032890 2017060790 2017071290 2016011590 2016062390 2016062890
Distribution pattern Nationally
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[26289]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1089-2018
Initiated October 23, 2017
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1089-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[45909]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
Code information IV4285 Lot codes: 2016032890 2016091290 2016112890
Distribution pattern Nationally
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[27032]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1090-2018
Initiated October 23, 2017
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1090-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[15033]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
Code information IV4690 Lot codes: 2015111690 2016012590 2016040490 2016082990 2016111490 2017010990 2017013090 2017052990 2017080790
Distribution pattern Nationally
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[27058]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1091-2018
Initiated October 23, 2017
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Convenience Kit containing components to assist practitioner with IV placement and securement.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1091-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[27608]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Convenience Kit containing components to assist practitioner with IV placement and securement.
Code information IV4885 IV5600 Lot codes: 2015090790 2015112390 2016012590 2016030790 2016052390 2016062790 2016080890 2017010290 2017013090 2017031390 2017052290 2015110201 2016010401 2016040401 2016061301 2016071101 2016082201 2017021601 2017041790 2017052290 2016122701 2015092801 2016022201 2017031301 2017062690
Distribution pattern Nationally
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[27194]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1092-2018
Initiated October 23, 2017
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Convenience Kit containing components to assist practitioner with IV placement and securement.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1092-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[45907]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Convenience Kit containing components to assist practitioner with IV placement and securement.
Code information IV5785 IV6135 Lot codes: 2015121890 2016031490 2016102490 2016111490 2017012390 2017050890 2016071190 2015101990 2015120790 2016010490 2016012590 2016101090 2017010290 2017061990 2017071090
Distribution pattern Nationally
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[27391]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1093-2018
Initiated October 23, 2017
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Convenience Kit containing components to assist practitioner with IV placement and securement.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1093-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[45905]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Convenience Kit containing components to assist practitioner with IV placement and securement.
Code information IV6860 IVS1345 Lot codes: 2015110290 2016011190 2016030790 2016050290 2016061390 2016081590 2016101090 2017010290 2017021390 2017032090 2017050890 2017071790 2015110990 2016020890 2016062090 2016071190 2016072590 2016080890 2016082990 2016090590 2016091990
Distribution pattern Nationally
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[27074]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1094-2018
Initiated October 23, 2017
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Convenience Kit containing components to assist practitioner with IV placement and securement.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1094-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[15035]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Convenience Kit containing components to assist practitioner with IV placement and securement.
Code information IVS1410 Lot codes: 2015120790 2016040490 2016092690 2017031390
Distribution pattern Nationally
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[26087]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1095-2018
Initiated October 23, 2017
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Convenience Kit containing components to assist practitioner with IV placement and securement.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1095-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[3129]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Convenience Kit containing components to assist practitioner with IV placement and securement.
Code information IVS425 Lot codes: 2016091290 2016082290
Distribution pattern Nationally
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[27345]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1096-2018
Initiated October 23, 2017
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Convenience Kit containing components to assist practitioner with IV placement and securement.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1096-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[27597]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Convenience Kit containing components to assist practitioner with IV placement and securement.
Code information MNS2790 Lot codes: 2016010490 2016033190 2016082990 2016120590 2017042090 2017090490
Distribution pattern Nationally
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[27373]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1097-2018
Initiated October 23, 2017
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Convenience Kit containing components to assist practitioner with IV placement and securement.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1097-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[32792]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Convenience Kit containing components to assist practitioner with IV placement and securement.
Code information SUT13705 Lot codes: 2016072190
Distribution pattern Nationally
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[26113]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1098-2018
Initiated October 23, 2017
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Convenience Kit containing components to assist practitioner with IV placement and securement.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1098-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[45903]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Convenience Kit containing components to assist practitioner with IV placement and securement.
Code information SUT8260A Lot codes: 2016070490 2016080590 2016112990 2017090690
Distribution pattern Nationally
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[27055]
FDA event record
· Exact recall-number query on openFDA
