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

Recall Z-0606-2016 — Baxter INTERLINK System, Y-Type Solution Set, 78 (2.0 m), 2 Injection Sites, Male Luer Lock Adapter, 1C8581 s, Product Usage: C8581: For the administration of fluids from a container into the patients vascular system through a vascular access device. .

U.S. FDA — Device Enforcement · United States · 2015-11-30 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0606-2016
Date of alert
2015-11-30
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Baxter Healthcare Corp.
Product category
device
Product type
Devices
Reported risk: Potential for dark loose particulate matter (400 microns or smaller) on the spike of the spike adapter or solution set.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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