FDA Device recall Z-2262-2024
BD Alaris System Manager REF: 9601, compatible with BD Alaris PC Units
- FDA Device
- Class II
- ongoing
- Published 2024-07-10
On 2024-07-10 the FDA classified a Class II recall of BD Alaris System Manager REF: 9601, compatible with BD Alaris PC Units by Carefusion 303, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2262-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-05-21 |
| Published | 2024-07-10 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Carefusion 303 |
| Distribution | US |
Product
BD Alaris System Manager REF: 9601, compatible with BD Alaris PC Units
Reason
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.
Identifiers
| code_info | UDI: 10885403960123/ Software versions 12.5.1 |
|---|
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-2262-2024%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.