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CareFusion 303, Inc. recalls BD Pyxis MedStation 4000 Main, REF 303
Recalled January 29, 2025 · FDA recall Z-0973-2025 · CareFusion 303
Hazard
Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure, Situation 2: Cable Ribbon Damage, Situation 3: Magnet Falling Out, · FDA Class II
Units
13055 units
Sold at
Worldwide
Description
Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure, Situation 2: Cable Ribbon Damage, Situation 3: Magnet Falling Out,
Product
BD Pyxis MedStation 4000 Main, REF 303
Manufacturer(s)
CareFusion 303, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →