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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K200304
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FDA Recall
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mC12-3 Transducer Probe 3 08/22/2025 Philips Ultrasound, Inc
mC7-2 Transducer Probe 3 08/22/2025 Philips Ultrasound, Inc
EPIQ CVxi Diagnostic Ultrasound Systems, Product Code: 795232 2 10/16/2021 Philips Ultrasound Inc
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