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

Recall Z-1595-2015 — 98" (249 cm) Transfer Set w/MicroClave T-Connector, 2 Check Valves, Luer Lock, Non-DEHP Tubing, Item No. B3372 Product Usage: IV Administration sets are intended for the infusion and withdrawal of fluids. The devices are provided sterile.

U.S. FDA — Device Enforcement · United States · 2015-04-20 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1595-2015
Date of alert
2015-04-20
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
ICU Medical, Inc.
Product category
device
Product type
Devices
Reported risk: ICU Medical is recalling MicroClave T-Connectors because they have potential connection separation issues that could lead to leakage.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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