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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 20 of 35 Results
510(K) Number: K213516
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Ingenia Elition S -For use as a diagnostic device to obtain cross-sectional images, spectroscopic im... 2 09/20/2024 Philips North America Llc
Ingenia Elition S Magnetic Resonance (MR) system, Product Numbers 781357 and 782106 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 S, Magnetic Resonance System. 2 04/17/2024 Philips North America Llc
Ingenia Elition X Magnetic Resonance (MR) system, Product Numbers 781358, 782107, and 782118 (SmartP... 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 X, Magnetic Resonance System. 2 04/17/2024 Philips North America Llc
Ingenia Elition X- For use as a diagnostic device to obtain cross-sectional images, spectroscopic im... 2 09/20/2024 Philips North America Llc
Intera 1.0T Omni/Stellar, Model Number: 781102; 2 05/15/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Intera 1.5T Master/Nova, Model Number: 781106; 2 05/15/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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