Drug recall
Siemens Mobilett Mira mobile x-ray system Product Usage: Mobile x-ray system
FDA recall event 62989 · Class II · Siemens Medical Solutions USA, Inc
Key facts
| Event ID | 62989 |
|---|---|
| Recall numbers | Z-2367-2012 |
| Recalling firm | Siemens Medical Solutions USA, Inc |
| Product type | Devices |
| Products | Siemens Mobilett Mira mobile x-ray system Product Usage: Mobile x-ray system |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | During regular product monitoring, firm became aware of a potential issue with the Mobilett Mira system, (serial numbers 1034, 1038, 1041, 1042, 1043, 1050, 1053, and 1054. During normal clinical… |
| Initiation date | Apr 30, 2012 |
| Report date | Sep 19, 2012 |
| Termination date | Sep 25, 2012 |
| 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: