FDA Device recall Z-1932-2024
BD Pyxis(TM) Anesthesia Station 4000, REF: 338
- FDA Device
- Class II
- ongoing
- Published 2024-06-05
On 2024-06-05 the FDA classified a Class II recall of BD Pyxis(TM) Anesthesia Station 4000, REF: 338 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-1932-2024 |
| 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(TM) Anesthesia Station 4000, REF: 338
Reason
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
Identifiers
| code_info | UDI: 10885403477829/ Serial Numbers provided 8/27/2025: 15549257 14897663 14895303 14895304 14895305 14895306 14895307…UDI: 10885403477829/ Serial Numbers provided 8/27/2025: 15549257 14897663 14895303 14895304 14895305 14895306 14895307 14895308 14895309 14895310 14895311 14877974 14819696 14956425 14956427 14956428 14956429 14956431 14956432 14622884 14622885 15091720 14546469 14361326 14361327 15019611 15019612 15019613 15019614 15019615 15019616 15019617 15019618 15019619 15019620 15289651 14558594 14558595 14558596 14558597 14558598 14558599 14558600 14558601 14558602 14558604 14558605 14558606 14558607 14384234 14384236 14384238 14384240 14384241 14384243 14384244 14384245 14384246 14384247 14384248 13932078 13932079 13932080 13932081 15507816 14379194 14379727 14379729 14379730 14379731 14379732 14379733 14379734 14379735 14379736 14379737 14379738 14379740 14379741 14379811 14379812 14379813 14379816 14379817 14379972 14379973 14379974 14379975 14379718 14379719 14379720 14379721 14379722 14379723 14379724 14379725 14379726 13859536 13859549 14544175 14544176 14544178 14544180 14544181 14567021 |
|---|
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-1932-2024%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.