BD Pyxis MedBank MedPass Software — Class II medical device recall Z-2646-2023
Ongoing recall by CareFusion 303, Inc., reported 2023-10-04, distributed in FL, KS, MI. After dispensing a timed dose medication for a patient, the automated dispensing cabinet software may continue
| Recall number | Z-2646-2023 |
|---|---|
| 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 | 2023-08-18 |
| Classified | 2023-09-28 |
| Reported by FDA | 2023-10-04 |
| Distributed | FL, KS, MI |
| Quantity | 37 |
| Reason classes | software |
| UPC / GTIN / UDI-DI | 10885403513817 |
| Model numbers | 139088-01 |
Product
BD Pyxis MedBank MedPass Software, REF: 139088-01
Reason for recall
After dispensing a timed dose medication for a patient, the automated dispensing cabinet software may continue to show the already dispensed medication dose is still available for dispense, which could lead to duplicate medication administration.
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-2646-2023. 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.