Drug recall
CIOS ALPHA; image intensified fluoroscopic x-ray system
FDA recall event 72138 · Class II · Siemens Medical Solutions USA, Inc
Key facts
| Event ID | 72138 |
|---|---|
| Recall numbers | Z-0118-2016 |
| Recalling firm | Siemens Medical Solutions USA, Inc |
| Product type | Devices |
| Products | CIOS ALPHA; image intensified fluoroscopic x-ray system |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | patient procedure interruption due to a potential system failure |
| Initiation date | Aug 17, 2015 |
| Report date | Nov 4, 2015 |
| Termination date | Dec 5, 2016 |
| 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: