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

Recall Z-1701-2023 — HydroSil Go Intermittent Urinary Catheters, Catalog Numbers: a) REF 71808, b) REF 71810, c) REF 71812, d) REF 71814, e) REF 71816, f) REF 71818

U.S. FDA — Device Enforcement · United States · 2023-04-20 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1701-2023
Date of alert
2023-04-20
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
C.R. Bard Inc
Product category
device
Product type
Devices
Reported risk: Some catheters had a manufacturing defect where the clear resealing label separating from the product foil pouch, resulting in a possible opening into the product packaging that could impact product sterility.
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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