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

Recall Z-2022-2014 — STOPCOCK EXT. SET W/ 3-WAY STOPCOCK WITH INJ. SITE AND SPINLOCK CONNECTOR, 22 inches and 37 inches

U.S. FDA — Device Enforcement · United States · 2014-05-29 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2022-2014
Date of alert
2014-05-29
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
B. Braun Medical, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
61356774
Reported risk: Complaints were received that reported the stopcock of some Stopcock Extension Sets are assembled in the reverse position, resulting in the stopcock being closed when set in the open position and vise versa.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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