BD Pyxis MedStation ES — Class II medical device recall Z-0670-2025
Ongoing recall by CareFusion 303, Inc., reported 2024-12-18, distributed nationwide. Due to a software issue, automated dispensing cabinet devices may open the wrong cubie pocket or position, whi
| Recall number | Z-0670-2025 |
|---|---|
| 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 | 2024-11-14 |
| Classified | 2024-12-11 |
| Reported by FDA | 2024-12-18 |
| Distributed | Nationwide (US) |
| Quantity | 98,526 |
| Reason classes | software |
| UPC / GTIN / UDI-DI | 10885403512667 |
| Model numbers | 323 |
Product
BD Pyxis MedStation ES, REF: 323
Reason for recall
Due to a software issue, automated dispensing cabinet devices may open the wrong cubie pocket or position, which can lead to: 1) Unintended and incorrect medication removal, or 2) Potential for a different medication (medication pulled in error) to be refilled/loaded, which may lead to may lead to low inventory or a stockout.
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-0670-2025. 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.