FDA Device recall Z-1928-2024
BD Pyxis MedStation 4000 System, REF: 303, 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 4000 System, REF: 303, 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-1928-2024 |
| 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 System, REF: 303, 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: 10885403512629/Serial numbers added 8/27/2025: 13811918 13811919 8000118765 8000118766 12761424 12761425 12740622…UDI: 10885403512629/Serial numbers added 8/27/2025: 13811918 13811919 8000118765 8000118766 12761424 12761425 12740622 12731265 12558708 15686451 15686452 15686453 15686454 15616386 15616388 15563539 15544140 15544141 15544142 15406815 15406817 15076403 15067076 15067081 15067083 15067085 15067088 15067091 15067095 15067096 15067098 15067099 15067100 15067103 15067104 15067108 15067109 15067110 15067111 15053373 15053374 15026036 15026038 14838460 14808782 14808783 14791224 14785171 14785172 14785173 14785174 14785175 14785176 14785177 14785178 14785179 14785180 14785181 14773852 14773853 14773855 14760077 14755527 14755528 14755529 14755530 14755531 14755532 14755533 14755534 14755535 14755536 14754778 14740957 14740958 14740959 14740960 14740961 14740962 14731697 14731699 14731700 14731701 14731702 14731703 14731704 14731705 14731706 14731707 14731708 14731709 14728147 14728148 14728149 14728150 14728151 14707852 14707853 14707854 14690161 14690162 14690163 14690165 14690167 1469016 |
|---|
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-1928-2024%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.