Medical Device Recalls
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1 to 10 of 22 Results
Related Medical Device Recalls |
Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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|---|---|---|---|
| Z-1659-2026 - Allura Xper FD10C; System Code: 722001; | 2 | 03/27/2026 |
FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Z-1680-2026 - Azurion 5 M20; System Code: (1)722228, (2)722232, (3) 722281 (OUS only); | 2 | 03/27/2026 |
FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Z-1661-2026 - ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722026; | 2 | 03/27/2026 |
FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Z-1662-2026 - ALLURA Xper FD10/10; System Code: (1) 722005, (2)722011, (3)722027; | 2 | 03/27/2026 |
FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Z-1663-2026 - ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028; | 2 | 03/27/2026 |
FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Z-1664-2026 - ALLURA Xper FD20 Biplane; System Code: (1) 722008, (2)722013; | 2 | 03/27/2026 |
FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Z-1665-2026 - ALLURA Xper FD20 OR Table; System Code: (1) 722015, (2)722023, (3)722035; | 2 | 03/27/2026 |
FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Z-1666-2026 - ALLURA Xper FD20 Biplane OR Table; System Code: (1) 722020, (2)722025; | 2 | 03/27/2026 |
FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Z-1667-2026 - ALLURA Xper FD10 OR Table; System Code: (1) 722022, (2)722033; | 2 | 03/27/2026 |
FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Z-1668-2026 - Allura Xper FD20/10; System Code: 722029; | 2 | 03/27/2026 |
FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
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