Class II

Medical Device Recall: BD Pyxis MedStation 4000 AUX, REF 306

CareFusion 303, Inc. · February 14, 2023

Reason for Recall

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,

Distribution

Worldwide

Quantity Affected

5056 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0974-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.