FDA Device recall Z-1930-2024
BD Pyxis MedStation 4000 7-Drawer Auxiliary Tower, REF: 306
- FDA Device
- Class II
- ongoing
- Published 2024-06-05
On 2024-06-05 the FDA classified a Class II recall of BD Pyxis MedStation 4000 7-Drawer Auxiliary Tower, REF: 306 by Carefusion 303, citing potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1930-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-04-15 |
| Published | 2024-06-05 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Carefusion 303 |
| Distribution | US |
Product
BD Pyxis MedStation 4000 7-Drawer Auxiliary Tower, REF: 306
Reason
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
Identifiers
| code_info | UDI: 10885403512636/Serial Numbers added 8/27/2025: 12558525 13351845 15616389 15616390 15616391 15563540 15544135 1554…UDI: 10885403512636/Serial Numbers added 8/27/2025: 12558525 13351845 15616389 15616390 15616391 15563540 15544135 15544136 15544137 15544138 15544139 15406818 15358663 15067079 15067087 15067090 15067097 15067101 15067102 15067106 15067107 14785182 14785183 14785184 14785185 14689030 14689031 14689033 14671361 14671362 14671363 14671364 14671365 14671366 14671367 14671369 14671370 14659569 14659570 14659571 14659572 14659573 14659574 14659576 14659577 14659578 14639957 14637299 14637300 14637301 14637302 14637303 14637304 14633430 14633431 14633432 14633433 14633434 14633435 14633436 14607306 14607307 14607308 14607309 14607310 14607311 14607312 14607313 14607314 14590696 14590697 14590698 14590699 14590700 14590702 14590703 14578551 14578552 14578553 14578554 14578555 14578556 14578558 14578559 14565988 14565989 14565990 14565991 14565992 14565993 14565994 14565995 14565996 14565997 14598309 15777264 15570731 15110842 14906229 14906231 14906233 14906235 14906237 14906238 14724865 147 |
|---|
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-1930-2024%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.