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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 14 Results
510(K) Number: K173451
 
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Ingenia Elition X (Product Number 781358) - HA FlexTrak II (Accessory Number 989710008732), patient ... 2 02/02/2024 Philips North America
Ingenia Elition X Magnetic Resonance (MR) system, Product Numbers 781358, 782107, and 782118 (SmartP... 2 08/11/2023 Philips North America
Ingenia Elition S Magnetic Resonance (MR) system, Product Numbers 781357 and 782106 2 08/11/2023 Philips North America
Ingenia Elition X Magnetic Resonance (MR) system, Product Numbers 781358, 782107, and 782118 (SmartP... 2 08/11/2023 Philips North America
Ingenia Elition S Magnetic Resonance (MR) system, Product Numbers 781357 and 782106 2 08/11/2023 Philips North America
Philips Upgrade to MR 7700 System, Model Number 782130 2 12/08/2022 Philips North America Llc
Philips MR 7700 System, Model Number 782120 2 12/08/2022 Philips North America Llc
Philips Ingenia Elition X MR System, Model Numbers 781358, 782107, 782119, 782136 2 12/08/2022 Philips North America Llc
Philips Ingenia Elition S MR System, Model Numbers 781357, 782106, 782137 2 12/08/2022 Philips North America Llc
Philips SmartPath to Ingenia Elition X MR System, Model Numbers 782118, 782132, 782144 2 12/08/2022 Philips North America Llc
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