Recall Z-0973-2025— CareFusion 303, Inc.
Class II · Ongoing
Class II FDA medical device recall by CareFusion 303, Inc., initiated 2023-02-14. FDA's recall record names no specific 510(k) clearance for this event. Product: BD Pyxis MedStation 4000 Main, REF 303. Reason: 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,.
- Recalling firm
- CareFusion 303, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2023-02-14
- Firm location
- San Diego, CA, United States
Product description
BD Pyxis MedStation 4000 Main, REF 303
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,
Data sourced from openFDA. This site is unofficial and independent of the FDA.