Medical Device Recalls
-
|
1 to 2 of 2 Results
Related Medical Device Recalls |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Z-2258-2026 - Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063, 722221), Azurion 3 M15 (722064, 722222), Azurion 5 M12 (722227), Azurion 5 M20 (722228), Azurion 7 B12 (722067, 722225),... | 2 | 05/28/2026 |
FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Z-2259-2026 - Allura system; System Code Description (Model Numbers): Allura Xper FD10 (722003, 722010, 722026), Allura Xper FD10 OR Table (722022, 722033), Allura Xper FD10/10 (722005, 722011, 722027), Allura Xper... | 2 | 05/28/2026 |
FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
-







