FDA Device recall Z-0976-2025
BD Pyxis Med 4000 Auxiliary (AUX), REF 314
- FDA Device
- Class II
- ongoing
- Published 2025-01-29
On 2025-01-29 the FDA classified a Class II recall of BD Pyxis Med 4000 Auxiliary (AUX), REF 314 by Carefusion 303, citing 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:….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0976-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-02-14 |
| Published | 2025-01-29 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Carefusion 303 |
| Distribution | n/a |
Product
BD Pyxis Med 4000 Auxiliary (AUX), REF 314
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,
Identifiers
| code_info | UDI/DI 10885403512650, Serial Numbers: 16140589, 16194078, 16194079, 16194081, 16079165. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0976-2025%22
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