FDA Device recall Z-1122-2025
BD Pyxis MedStation ES (Med ES Main) REF: 323
- FDA Device
- Class II
- ongoing
- Published 2025-02-19
On 2025-02-19 the FDA classified a Class II recall of BD Pyxis MedStation ES (Med ES Main) REF: 323 by Carefusion 303, citing retroactive-Due to increase in complaints, their is a potential for drawer and/or door failures of the medication cabinet which could result in delay in accessing medications.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1122-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-02-23 |
| Published | 2025-02-19 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Carefusion 303 |
| Distribution | US |
Product
BD Pyxis MedStation ES (Med ES Main) REF: 323. Intended to securely store and dispense medications to a qualified and authorized healthcare provider.
Reason
Retroactive-Due to increase in complaints, their is a potential for drawer and/or door failures of the medication cabinet which could result in delay in accessing medications.
Identifiers
| code_info | UDI: 0885403212667/Serial Numbers: 16160944 16142237 16188205 16188207 16188212 16188216 16188220 16188229 16130230 161…UDI: 0885403212667/Serial Numbers: 16160944 16142237 16188205 16188207 16188212 16188216 16188220 16188229 16130230 16130231 16183872 16184152 16180604 16155071 16172476 16161355 16184716 16184717 16155208 16155209 16155210 16155211 16155212 16155213 16156000 16156004 16156006 16156008 16156018 16145933 16180546 16180547 16180548 16161088 16183862 16173683 16173684 16173685 16173686 16173687 16173696 16173698 16173701 16173702 16173703 16168000 16173704 16173705 16164513 16164517 16155941 16155943 16167578 15925963 16145929 16145930 16130236 16145931 16145932 16183776 16183781 16183784 16183789 16183792 16183801 16183804 16161294 16184711 16184713 16187331 16190475 16161087 16173513 16173514 16173515 16179685 16173518 16179683 16173529 16179596 16168002 16177915 16188887 16177921 16190561 16185661 16185662 16188555 16188556 16188557 16188558 16188559 16188562 16188564 16188565 16188566 16188567 16188568 16188569 16188570 16188571 16173435 16173436 16173438 16173440 16160946 16161016 16 |
|---|
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-1122-2025%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.