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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 9 of 9 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-1928-2025 - Achieva XR Product Numbers: (1) 781153, (2) 781253; 2 06/09/2025 FEI # 3006648320
Philips North America
Z-1929-2025 - Intera 1.5T Achieva IT Nova Product Number: 781175 2 06/09/2025 FEI # 3006648320
Philips North America
Z-1930-2025 - Intera 1.5T Achieva Nova Product Number: 781172; 2 06/09/2025 FEI # 3006648320
Philips North America
Z-1931-2025 - Intera 1.5T Achieva Nova-Dual Product Number: 781173; 2 06/09/2025 FEI # 3006648320
Philips North America
Z-1932-2025 - Intera 1.5T Explorer/Nova Dual Product Number: 781108; 2 06/09/2025 FEI # 3006648320
Philips North America
Z-1933-2025 - Intera 1.5T Master/Nova Product Number: 781106; 2 06/09/2025 FEI # 3006648320
Philips North America
Z-1934-2025 - Intera 1.5T Omni/Stellar; Product Number: 781104; 2 06/09/2025 FEI # 3006648320
Philips North America
Z-1935-2025 - Intera Achieva 1.5T Pulsar; Product Number: 781171; 2 06/09/2025 FEI # 3006648320
Philips North America
Z-1936-2025 - SmartPath to dStream for 1.5T®; Product Number: 782146; 2 06/09/2025 FEI # 3006648320
Philips North America
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