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U.S. Department of Health and Human Services

Medical Device Recalls

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Related Medical Device Recalls
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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Z-2395-2023 - Ingenia Elition X Magnetic Resonance (MR) system, Product Numbers 781358, 782107, and 782118 (SmartPath to Ingenia Elition X) 2 08/11/2023 Philips North America
Z-2397-2023 - MR 7700 Magnetic Resonance (MR) system, Product Numbers 782120 and 782130 (Upgrade to MR 7700) 2 08/11/2023 Philips North America
Z-2396-2023 - Ingenia Elition S Magnetic Resonance (MR) system, Product Numbers 781357 and 782106 2 08/11/2023 Philips North America
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