BD Pyxis MedStation ES (Med ES Main), REF 323 — recall Z-0971-2025
U.S. FDA — Device Enforcement · United States · 2023-02-14 · Class II
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Reported risk: 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,
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