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CareFusion 303, Inc. recalls Alaris Pump VersaSafe Infusion Set, Model No. 2122-0007
Recalled March 23, 2016 · FDA recall Z-1179-2016 · CareFusion 303
Hazard
CareFusion is recalling the Alaris VersaSafe Infusion Set because of separation and/or leakages at the VersaSafe split septum port and tubing may lead to leakage of the administration set. · FDA Class II
Units
5,760 units
Sold at
Michigan
Description
CareFusion is recalling the Alaris VersaSafe Infusion Set because of separation and/or leakages at the VersaSafe split septum port and tubing may lead to leakage of the administration set.
Product
Alaris Pump VersaSafe Infusion Set, Model No. 2122-0007
Manufacturer(s)
CareFusion 303, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →