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Baxter Healthcare Corp. recalls Dual Luer Lock Cap The device is intended for use as a cap for male or female Luer ports on medical devices such as m
Recalled November 13, 2013 · FDA recall Z-0143-2014 · Baxter Healthcare
Hazard
The firm is recalling lots 10043 and 10044 due to loose particulate matter found in the packaging. Particulate matter entering the fluid path from the Luer lock caps may result in embolic events. · FDA Class II
Units
628,992 units
Sold at
Worldwide Distribution - USA (nationwide) and the country of Canada.
Description
The firm is recalling lots 10043 and 10044 due to loose particulate matter found in the packaging. Particulate matter entering the fluid path from the Luer lock caps may result in embolic events.
Product
Dual Luer Lock Cap The device is intended for use as a cap for male or female Luer ports on medical devices such as manifolds, stopcocks or sets.
Manufacturer(s)
Baxter Healthcare Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →