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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 18 of 18 Results
Related Medical Device Recalls
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Z-1798-2025 - Product Name: Ingenia Ambition S; Model Numbers: (1) 781359, (2) 782108, (3) 782139; 2 05/16/2025 FEI # 3016618143
Philips North America Llc
Z-1799-2025 - Product Name: Ingenia 1.5T CX; Model Number: 781262; 2 05/16/2025 FEI # 3016618143
Philips North America Llc
Z-1800-2025 - Product Name: Ingenia 3.0T CX; Model Number: 781271; 2 05/16/2025 FEI # 3016618143
Philips North America Llc
Z-1801-2025 - Product Name: Ingenia Ambition X; Model Numbers: (1) 781356, (2) 782109, (3) 782138; 2 05/16/2025 FEI # 3016618143
Philips North America Llc
Z-1802-2025 - Product Name: Ingenia Elition S; Model Numbers: (1) 781357, (2) 782106, (3) 782137; 2 05/16/2025 FEI # 3016618143
Philips North America Llc
Z-1803-2025 - Product Name: Ingenia Elition X; Model Numbers: (1) 781358, (2) 782107, (3) 782136; 2 05/16/2025 FEI # 3016618143
Philips North America Llc
Z-1804-2025 - Product Name: MR 5300; Model Numbers: (1) 782110, (2) 782152; 2 05/16/2025 FEI # 3016618143
Philips North America Llc
Z-1789-2025 - Product Name: SmartPath to dStream for 3.0T; Model Number: 782145 2 05/16/2025 FEI # 3016618143
Philips North America Llc
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