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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K081802
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Recall
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FDA Recall
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D2cwc Transducer Probe 3 08/22/2025 Philips Ultrasound, Inc
Philips S5-1 Transducer. 2 07/02/2025 Philips Ultrasound, Inc
Philips X7-2t Transducer. 2 07/02/2025 Philips Ultrasound, Inc
X7-2t Transducer Probe 3 08/22/2025 Philips Ultrasound, Inc
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