Medical Device Recalls
-
|
1 to 5 of 5 Results
510(K) Number: K111912 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Mobilett Mira wireless (VA20) mobile x-ray system(s) | 2 | 11/14/2023 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| Mobiletta Mira Mobile X-ray System | 2 | 08/05/2013 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| Siemens Mobilette Mira, intended use as Mobile x-ray system. | 2 | 12/06/2012 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| Siemens Mobilett Mira mobile x-ray system Product Usage: Mobile x-ray system | 2 | 09/11/2012 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| Siemens Mobilett Mira. Mobile X-Ray System. | 2 | 09/06/2012 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
-







