Medical Device Recalls
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91 to 100 of 500 Results
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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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| ALLURA Xper FD10/10; System Code: (1) 722005, (2)722011, (3)722027; | 2 | 03/27/2026 |
FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028; | 2 | 03/27/2026 |
FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| ALLURA Xper FD20 Biplane; System Code: (1) 722008, (2)722013; | 2 | 03/27/2026 |
FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| 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. |
| ALLURA Xper FD20 Biplane OR Table; System Code: (1) 722020, (2)722025; | 2 | 03/27/2026 |
FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| ALLURA Xper FD10 OR Table; System Code: (1) 722022, (2)722033; | 2 | 03/27/2026 |
FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Allura Xper FD20/10; System Code: 722029; | 2 | 03/27/2026 |
FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Allura Xper FD20/20 OR Table; System Code: 722039; | 2 | 03/27/2026 |
FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Allura Xper FD20/15; System Code: 722058; | 2 | 03/27/2026 |
FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Allura Xper FD20/15 OR Table; System Code: 722059; | 2 | 03/27/2026 |
FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| * The maximium 500 devices meeting your search criteria returned. Please narrow your search. |
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