FDA Device recall Z-1931-2024
BD Pyxis" Anesthesia Station ES, REF: 327
- FDA Device
- Class II
- ongoing
- Published 2024-06-05
On 2024-06-05 the FDA classified a Class II recall of BD Pyxis" Anesthesia Station ES, REF: 327 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-1931-2024 |
| 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" Anesthesia Station ES, REF: 327
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: 15662739 15662740 15662741 15662743 15662745 15662746 15662747 1566…UDI: 10885403512636/Serial numbers added 8/27/2025: 15662739 15662740 15662741 15662743 15662745 15662746 15662747 15662749 15662752 15662753 15662754 15662756 15662758 15662759 15662760 15662761 15662762 15662763 15662764 15662765 15662767 15662768 15662769 15662770 15662771 15662772 15662773 15662774 15662775 15375059 15757979 15757980 15755213 15755214 15755215 15755216 15755217 15755218 15022893 15022894 15022895 15022896 14284496 14284498 17700227 17414413 17276726 17215411 15689985 15689986 15566064 15566065 15566067 15566068 15566069 15566070 15566071 15566072 15566073 15566074 15566075 15566076 15566077 15566078 15566079 15540267 15540268 15540270 15540271 15540272 15540273 15540274 15540276 15540277 15540278 15540279 15540280 15540282 15540283 15540284 15540285 15519753 15519754 15519755 15519756 15519757 15519758 15519759 15519760 15519761 15519762 15519763 15519764 15519765 15519766 15519767 15503435 15503437 15503439 15503441 15503443 15503444 15503445 15503447 15503448 155 |
|---|
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-1931-2024%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.