BD Pyxis MedStation Auxiliary ES REF: 324 — Class II medical device recall Z-1123-2025
Ongoing recall by CareFusion 303, Inc., reported 2025-02-19, distributed nationwide. Retroactive-Due to increase in complaints, their is a potential for drawer and/or door failures of the medicat
| Recall number | Z-1123-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | CareFusion 303, Inc., San Diego, CA, United States |
| Recall initiated | 2024-02-23 |
| Classified | 2025-02-11 |
| Reported by FDA | 2025-02-19 |
| Distributed | Nationwide (US) |
| UPC / GTIN / UDI-DI | 10885403512681 |
| Serial numbers | 15638516, 15638517, 15638520, 15863156, 15917861, 15917863, 15955141, 15998618, 15998620, 15998621, 15998622, 15998624, 15998625, 15998626, 15998627, 15998628, 15998629, 15998630, 16003148, 16010058, 16010059, 16010060, 16010061, 16010062, 16010063 and 475 more |
| Model numbers | 324 |
Product
BD Pyxis MedStation Auxiliary ES REF: 324. Intended to securely store and dispense medications to a qualified and authorized healthcare provider.
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1123-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.