FDA Device recall Z-1927-2024
BD Pyxis MedStation ES, REF: 323, Medication Cabinet
- FDA Device
- Class II
- ongoing
- Published 2024-06-05
On 2024-06-05 the FDA classified a Class II recall of BD Pyxis MedStation ES, REF: 323, Medication Cabinet 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-1927-2024 |
| 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 ES, REF: 323, Medication Cabinet
Reason
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
Identifiers
| code_info | UDI: 10885403512667/New Serial Numbers reported 8/27/25: 14879021 15683381 15683382 15683385 15683386 15683387 15683388…UDI: 10885403512667/New Serial Numbers reported 8/27/25: 14879021 15683381 15683382 15683385 15683386 15683387 15683388 15683389 15683390 15674988 15674992 15674993 15674994 15674995 15674996 15674998 15674999 15675000 15675001 15675036 15758077 15758078 15758079 15755497 15755499 15755501 15754424 17269762 13625680 13625681 13625682 13625684 13611196 13611198 13611204 13467008 13336011 13336013 13336014 13336015 13336016 14386862 14265629 14265630 14202688 14202689 14202690 14202691 14202692 14194839 14194841 14194842 14157202 14157203 14157204 14157205 14157206 14157207 14157208 14157209 14157210 14157211 14157212 13785825 13593077 13192143 13137112 13074966 13074968 13055699 13055700 13055726 13054792 13054060 13054061 13054101 12698939 17332556 17122344 16995995 16995997 16995998 16996016 16747803 16747804 16747805 16747843 16747844 16747988 15616385 15664565 15607464 15607465 15607466 15607495 15607497 15607498 15607499 15607501 15607503 15604320 15604321 15604323 15604324 1560432 |
|---|
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-1927-2024%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.