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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K231190
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FDA Recall
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Philips Affiniti 70, Diagnostic Ultrasound System Model # 795210 2 11/09/2023 Philips Ultrasound, Inc.
Philips EPIQ Diagnostic Ultrasound System Models: EPIQ 7G(model # 795200), EPIQ 7C (Model # 795201)... 2 11/09/2023 Philips Ultrasound, Inc.
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