Medical Device Recalls
-
|
1 to 10 of 14 Results
Related Medical Device Recalls |
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Z-1783-2025 - SmartPath to dStream for 3.0T, Model Number: 782145; | 2 | 05/15/2025 |
FEI # 3002807880 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Z-1782-2025 - SmartPath to dStream for 1.5T, Model Number: 782146; | 2 | 05/15/2025 |
FEI # 3002807880 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Z-1781-2025 - Intera CV, Model Number: 781107; | 2 | 05/15/2025 |
FEI # 3002807880 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Z-1780-2025 - Intera 3.0T Quasar Dual, Model Number: 781150; | 2 | 05/15/2025 |
FEI # 3002807880 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Z-1774-2025 - Intera 1.5T, Model Numbers: 781195 and 781295; | 2 | 05/15/2025 |
FEI # 3002807880 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Z-1779-2025 - Intera 1.5T R11, Model Number: 781170; | 2 | 05/15/2025 |
FEI # 3002807880 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Z-1778-2025 - Intera 1.5T Power/Pulsar, Model Number: 781105; | 2 | 05/15/2025 |
FEI # 3002807880 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Z-1777-2025 - Intera 1.5T Omni/Stellar, Model Number: 781104; | 2 | 05/15/2025 |
FEI # 3002807880 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Z-1776-2025 - Intera 1.5T Master/Nova, Model Number: 781106; | 2 | 05/15/2025 |
FEI # 3002807880 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Z-1775-2025 - Intera 1.5T Explorer/Nova Dual, Model Number: 781108; | 2 | 05/15/2025 |
FEI # 3002807880 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
-







