Data Foundry

Medical device recalls 2015

Bard Peripherally Inserted Central Catheter — Class II medical device recall Z-1443-2015

Terminated recall by Bard Access Systems, reported 2015-04-22, distributed nationwide. Potential for inadvertent scalpel stick injury involving the safety scalpel.

Recall numberZ-1443-2015
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmBard Access Systems, Salt Lake City, UT, United States
Recall initiated2014-06-24
Classified2015-04-13
Reported by FDA2015-04-22
Terminated2015-11-05
DistributedNationwide (US)
Quantity51,025 units
Lot numbers1174108, 1174108D, 1175108, 1194108, 1194108D, 1194118, 1275108, 1275108D, 1295108, 1295108D, 1295108FD, 1295118, 1385108Q, 1385108QD, 1386108, 1386108D, 1395108QD, 1396118, 2194108, 2295108, 3154108, 3174108, 3174108D, 3175108, 3194108, 3194108D, 3255108, 3274108, 3275108, 3275108D, 3295108, 3295108D, 3295108FD, 3385108Q, 3385108QD, 3386108, 3386108D, 3395108Q, 3395108QD, 3396108 and 32 more

Product

Bard Peripherally Inserted Central Catheter (PICC) and Dialysis catheter kits containing Safe-Cut Safety Scalpels.

Reason for recall

Potential for inadvertent scalpel stick injury involving the safety scalpel.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1443-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.