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

Recall Z-2006-2025 — REF: 381923 BD Insyte Autoguard Winged Shielded IV Catheter, 22 GA x 1.00 in (0.9 x 25 mm) 35 mL/min, STERILEEO, RxOnly

U.S. FDA — Device Enforcement · United States · 2025-05-21 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2006-2025
Date of alert
2025-05-21
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Becton Dickinson Infusion Therapy Systems, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
382903819232
Reported risk: Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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