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

Recall Z-1871-2025 — Catalog No. 8888160325; Umbilical Vessel Catheter 2.5 French single lumen

U.S. FDA — Device Enforcement · United States · 2025-05-02 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1871-2025
Date of alert
2025-05-02
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Cardinal Health 200, LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10192253040296
Reported risk: Packaging defect may compromise sterility of the product. Use of a non-sterile product on the patient could lead to infection in neonates.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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