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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 19 Results
Related Medical Device Recalls
 
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Product Description
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Z-2200-2025 - Achieva 3.0T; Model Numbers (REF): (1) 781177, (2) 781277, (3) 781278, (4) 781344, (5) 781345; 2 07/30/2025 Philips North America
Z-2218-2025 - Upgrade to MR 7700 Model Number (REF): 782130; 2 07/30/2025 Philips North America
Z-2202-2025 - Evolution Upgrade 1.5T Model Numbers (REF): (1) 782116, (2) 782148; 2 07/30/2025 Philips North America
Z-2203-2025 - Evolution Upgrade 3.0T Model Numbers (REF): (1) 782117, (2) 782143; 2 07/30/2025 Philips North America
Z-2204-2025 - Ingenia 1.5T Model Numbers (REF): (1) 781315, (2) 718641, (3) 781396, (4) 782101, (5) 782115, (6) 782140; 2 07/30/2025 Philips North America
Z-2205-2025 - Ingenia 1.5T S Model Number (REF): 781347; 2 07/30/2025 Philips North America
Z-2206-2025 - Ingenia 3.0T Model Numbers (REF): (1) 781342, (2) 781377, (3) 782103; 2 07/30/2025 Philips North America
Z-2207-2025 - Ingenia 3.0T CX Model Numbers (REF): (1) 781271, (2) 782105; 2 07/30/2025 Philips North America
Z-2208-2025 - Ingenia Ambition S Model Numbers (REF): (1) 781359, (2) 782108, (3) 782133 (China ONLY), (4) 782139; 2 07/30/2025 Philips North America
Z-2209-2025 - Ingenia Ambition X Model Numbers (REF): (1) 781356, (2) 782109, (3) 782138; 2 07/30/2025 Philips North America
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