FDA Device recall Z-0971-2025
BD Pyxis MedStation ES (Med ES Main), REF 323
- FDA Device
- Class II
- ongoing
- Published 2025-01-29
On 2025-01-29 the FDA classified a Class II recall of BD Pyxis MedStation ES (Med ES Main), REF 323 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-0971-2025 |
| 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 MedStation ES (Med ES Main), REF 323
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 10885403212667, Serial Numbers: 12439897, 12440725, 12440974, 12440975, 12441103, 12441333, 12441432, 12447684,…UDI/DI 10885403212667, Serial Numbers: 12439897, 12440725, 12440974, 12440975, 12441103, 12441333, 12441432, 12447684, 12451247, 12451619, 12455492, 12455493, 12455498, 12455793, 12456970, 12463612, 12469470, 12469471, 12469488, 12470842, 12474026, 12476547, 12483201, 12483203, 12483393, 12483402, 12486737, 12499043, 12499616, 12499617, 12499618, 12499838, 12501936, 12502072, 12502073, 12502074, 12502075, 12502076, 12502077, 12502078, 12502079, 12502080, 12504784, 12505982, 12507257, 12507258, 12507411, 12508303, 12510196, 12511166, 12511167, 12511168, 12511169, 12511170, 12511171, 12511172, 12511173, 12511174, 12511933, 12511934, 12511935, 12514265, 12514266, 12514267, 12515355, 12515356, 12515357, 12515358, 12515360, 12515364, 12515366, 12519098, 12522942, 12524481, 12527930, 12528709, 12528710, 12530090, 12531297, 12531298, 12531352, 12531353, 12531354, 12531414, 12531415, 12531416, 12531417, 12531418, 12531420, 12531421, 12531422, 12531423, 12540194, 12540196, 12540267, 12540268, |
|---|
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-0971-2025%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.