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CareFusion 303, Inc. recalls Trifurcated Extension Set, model no. ME 1224. Trifurcated Extension Set, model no. MP 9230.
Recalled February 12, 2014 · FDA recall Z-0931-2014 · CareFusion 303
Hazard
CareFusion is recalling the Trifurcated Extension Set, models ME 1224 and MP 9230, because they may have a defect in the trifurcated component that could result in a component leak. · FDA Class II
Units
9,550 units
Sold at
Nationwide in US and Canada
Description
CareFusion is recalling the Trifurcated Extension Set, models ME 1224 and MP 9230, because they may have a defect in the trifurcated component that could result in a component leak.
Product
Trifurcated Extension Set, model no. ME 1224. Trifurcated Extension Set, model no. MP 9230.
Manufacturer(s)
CareFusion 303, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →