BD Alaris System Manager REF: 9601 — Class II medical device recall Z-2262-2024
Ongoing recall by CareFusion 303, Inc., reported 2024-07-10, distributed nationwide. Due to a software issue the PC unit may not connect to the server which could impact wireless data transmissio
| Recall number | Z-2262-2024 |
|---|---|
| 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 | 2024-05-21 |
| Classified | 2024-07-03 |
| Reported by FDA | 2024-07-10 |
| Distributed | Nationwide (US) |
| Quantity | 168 software |
| Reason classes | software |
| UPC / GTIN / UDI-DI | 10885403960123 |
| Model numbers | 9601 |
Product
BD Alaris System Manager REF: 9601, compatible with BD Alaris PC Units
Reason for recall
Due to a software issue the PC unit may not connect to the server which could impact wireless data transmission to and from the server.
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-2262-2024. 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.