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Baxter Healthcare Corp. recalls Baxter INTERLINK System, Y-Type Solution Set, 78 (2.0 m), 2 Injection Sites, Male Luer Lock Adapter, 1C8581 s, Produc
Recalled January 13, 2016 · FDA recall Z-0606-2016 · Baxter Healthcare
Hazard
Potential for dark loose particulate matter (400 microns or smaller) on the spike of the spike adapter or solution set. · FDA Class II
Units
9600 units
Sold at
US Nationwide Distribution and the country of Canada
Description
Potential for dark loose particulate matter (400 microns or smaller) on the spike of the spike adapter or solution set.
Product
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. .
Manufacturer(s)
Baxter Healthcare Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →