FDA Device recall Z-1278-2016
Cios Alpha, mobile X-ray system
- FDA Device
- Class II
- terminated
- Published 2016-04-06
On 2016-04-06 the FDA classified a Class II recall of Cios Alpha, mobile X-ray system by Siemens Medical Solutions Usa, citing software issues on Cios Alpha mobile C-Arm system.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1278-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-02-19 |
| Published | 2016-04-06 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
Cios Alpha, mobile X-ray system
Reason
Software issues on Cios Alpha mobile C-Arm system
Identifiers
| code_info | Model # 10308191 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1278-2016%22
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