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

Recall Z-1431-2021 — Bard Clean-Cath Intermittent Catheter, 12 French female length (catheter, urological) - Product Usage: for urological use only.

U.S. FDA — Device Enforcement · United States · 2021-01-11 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1431-2021
Date of alert
2021-01-11
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
C.R. Bard, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00801741038730
Reported risk: The device catheter tip was cut off (no tip) and the product packaging was not fully sealed.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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