Drug recall
Cios Alpha, mobile X-ray system
FDA recall event 73605 · Class II · Siemens Medical Solutions USA, Inc
Key facts
| Event ID | 73605 |
|---|---|
| Recall numbers | Z-1278-2016 |
| Recalling firm | Siemens Medical Solutions USA, Inc |
| Product type | Devices |
| Products | Cios Alpha, mobile X-ray system |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Software issues on Cios Alpha mobile C-Arm system |
| Initiation date | Feb 19, 2016 |
| Report date | Apr 6, 2016 |
| Termination date | Mar 20, 2017 |
| City | Malvern |
| State | PA |
| Country | United States |
| FEI number | 2240869 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: