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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K230972
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Ingenia Elition X Model Numbers (REF): (1) 781358, (2) 782107, (3) 782119, (4) 782136, (5) 782151 (... 2 07/30/2025 Philips North America
Ingenia Elition S Model Numbers (REF): (1) 781357, (2) 782106, (3) 782137, (4) 782150 (China ONLY); 2 07/30/2025 Philips North America
MR 7700 Model Numbers (REF): (1) 782120, (2) 782153; 2 07/30/2025 Philips North America
Product Name: Ingenia Elition X; Model Numbers: (1) 781358, (2) 782107, (3) 782136; 2 05/16/2025 Philips North America Llc
Product Name: Ingenia Elition S; Model Numbers: (1) 781357, (2) 782106, (3) 782137; 2 05/16/2025 Philips North America Llc
Product Name: Upgrade to MR 7700; Model Number: 782130; 2 05/16/2025 Philips North America Llc
Product Name: MR 7700; Model Numbers: (1) 782120, (2) 782153; 2 05/16/2025 Philips North America Llc
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