FDA Device recall Z-0973-2025
BD Pyxis MedStation 4000 Main, REF 303
- FDA Device
- Class II
- ongoing
- Published 2025-01-29
On 2025-01-29 the FDA classified a Class II recall of BD Pyxis MedStation 4000 Main, REF 303 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-0973-2025 |
| 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 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,
Identifiers
| code_info | UDI/DI 10885403512629, Serial Numbers: 12439536, 12439538, 12439539, 12439540, 12439541, 12439544, 12440786, 12440787,…UDI/DI 10885403512629, Serial Numbers: 12439536, 12439538, 12439539, 12439540, 12439541, 12439544, 12440786, 12440787, 12440788, 12440789, 12440790, 12440791, 12440792, 12440978, 12440979, 12441431, 12443165, 12446066, 12448071, 12448072, 12448073, 12448074, 12448142, 12450907, 12450908, 12450909, 12450910, 12450911, 12450912, 12450913, 12450914, 12450915, 12450968, 12450970, 12450971, 12450973, 12450974, 12450975, 12450976, 12451251, 12451628, 12452651, 12452991, 12452993, 12453011, 12453012, 12453013, 12455427, 12455859, 12457587, 12457588, 12457589, 12457590, 12459775, 12461364, 12461365, 12461368, 12461369, 12461516, 12461517, 12461518, 12461520, 12462977, 12462978, 12463388, 12465197, 12465198, 12465199, 12465200, 12466882, 12468231, 12468628, 12470401, 12470403, 12470405, 12470879, 12471080, 12471091, 12471093, 12471094, 12471098, 12471103, 12472362, 12472380, 12472381, 12477309, 12477310, 12477311, 12477771, 12478580, 12479700, 12479701, 12479702, 12479703, 12479722, 12479731, |
|---|
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-0973-2025%22
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