FDA Device recall Z-1929-2024
BD Pyxis" MedStation ES 7-Drawer Auxiliary Tower, REF: 324
- 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 7-Drawer Auxiliary Tower, REF: 324 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-1929-2024 |
| 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 7-Drawer Auxiliary Tower, REF: 324
Reason
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
Identifiers
| code_info | UDI: 10885403512681/ Serial Numbers as of 8/27/2025:15674986 15674990 15674991 15674997 15758081 15758083 15755500 1728…UDI: 10885403512681/ Serial Numbers as of 8/27/2025:15674986 15674990 15674991 15674997 15758081 15758083 15755500 17280396 17275260 17275265 13611197 13611199 13611203 13467012 13336012 13336017 13336018 13336019 14386863 14265628 14194837 14157188 14157189 14157190 14157191 14157192 14157193 14157196 14157198 14157201 17578908 17578909 17338468 16726578 16726580 15222318 15222321 15284383 15222317 15167680 15167681 14823787 14648430 14648434 14648435 14639939 14639943 14639161 14639163 14639317 14634512 14634513 14634707 14634708 14634277 14630544 14629428 14539222 14537575 14537577 14537582 14537585 14537586 14537588 14518472 14522389 14522394 14522395 14522396 14522400 14522404 14522411 14522412 14522413 14522414 14522415 14522432 14522433 14522434 14522439 15686444 17437605 17437607 15576824 15558601 15554968 15554969 15548934 15597853 15597854 14677986 14672121 14672122 14672123 14671340 14671341 14671342 14671343 14666864 14666865 14666866 14666867 14663588 14657424 14655523 146 |
|---|
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-1929-2024%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.