Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1994-2021 — 5 Fr IR PowerPICC Convenience Kit Catheter Dual Lumen with 70 cm Guidewire Unit Label: PowerPICC REF CK000340B BARD MYPICC KIT 5F French Size Dual-Lumen 70cm Guidewire

U.S. FDA — Device Enforcement · United States · 2021-05-19 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1994-2021
Date of alert
2021-05-19
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Bard Access Systems Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00801741126697
Reported risk: Catheter convenience kits contain the incorrect guidewire. Kits were labeled with 70cm guidewires, but contained a 50cm guidewire.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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