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U.S. Department of Health and Human Services

Medical Device Recalls
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81 to 90 of 500 Results *
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Product Description
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Recall
Class
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FDA Recall
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Azurion 5 M12; System Code: (1)722227, (2)722231; 2 03/27/2026 FEI # 3042175844
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Azurion 7 M20; System Code: (1)722079, (2)722224, (3)722234, (4)722282 (OUS only); 2 03/27/2026 FEI # 3042175844
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Azurion 7 M12; System Code: (1)722078, (2)722223, (3)722233; 2 03/27/2026 FEI # 3042175844
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Azurion 7 B20; System Code: (1)722068, (2)722226, (3)722236; 2 03/27/2026 FEI # 3042175844
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Azurion 7 B12; System Code: (1)722067, (2)722225, (3)722235; 2 03/27/2026 FEI # 3042175844
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Azurion 3 M15; System Code: (1)722064, (2)722222, (3)722230, (4)722280 (OUS Only); 2 03/27/2026 FEI # 3042175844
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Azurion 3 M12; System Code: (1)722063, (2)722221, (3)722229; 2 03/27/2026 FEI # 3042175844
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD10C; System Code: 722001; 2 03/27/2026 FEI # 3042175844
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
ALLURA Xper FD10F; System Code: 722002; 2 03/27/2026 FEI # 3042175844
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722026; 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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