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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: K014191
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FDA Recall
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7.5MHZ Endo Transducer Probe 3 08/22/2025 Philips Ultrasound, Inc
OMNI III TEE Transducer Probe 3 08/22/2025 Philips Ultrasound, Inc
OMNI II TEE Transducer Probe 3 08/22/2025 Philips Ultrasound, Inc
Envisor, M2540 Diagnostic Ultrasound System 2 06/22/2005 Philips Ultrasound, Inc.
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