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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 17 Results
510(K) Number: K212673
 
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MR 5300 Model Numbers (REF): (1) 782110, (2) 782135 (China ONLY), (3) 782152; 2 07/30/2025 Philips North America
Product Name: MR 5300; Model Numbers: (1) 782110, (2) 782152; 2 05/16/2025 Philips North America Llc
Ingenia 3.0T - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images... 2 09/20/2024 Philips North America Llc
Ingenia 3.0T CX - For use as a diagnostic device to obtain cross-sectional images, spectroscopic ima... 2 09/20/2024 Philips North America Llc
Ingenia Ambition S - For use as a diagnostic device to obtain cross-sectional images, spectroscopic ... 2 09/20/2024 Philips North America Llc
Ingenia Ambition X - For use as a diagnostic device to obtain cross-sectional images, spectroscopic... 2 09/20/2024 Philips North America Llc
Ingenia 1.5T -For use as a diagnostic device to obtain cross-sectional images, spectroscopic images ... 2 09/20/2024 Philips North America Llc
Evolution Upgrade 3.0T - For use as a diagnostic device to obtain cross-sectional images, spectrosco... 2 09/20/2024 Philips North America Llc
Ingenia Elition S -For use as a diagnostic device to obtain cross-sectional images, spectroscopic im... 2 09/20/2024 Philips North America Llc
SmartPath to Ingenia Elition X - For use as a diagnostic device to obtain cross-sectional images, sp... 2 09/20/2024 Philips North America Llc
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