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U.S. Department of Health and Human Services

Medical Device Recalls

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11 to 20 of 31 Results
510(K) Number: K013153
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Product Description
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FDA Recall
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HYDRATOME RX 44-30MM/260CM Material Number: M00583050 2 03/11/2022 Boston Scientific Corporation
HYDRATOME RX 44-30MM/450CM Material Number: M00583070 2 03/11/2022 Boston Scientific Corporation
HYDRATOME RX 49-20MM/260CM Material Number: M00583000 2 03/11/2022 Boston Scientific Corporation
HYDRATOME RX 49-30MM/260CM Material Number: M00583010 2 03/11/2022 Boston Scientific Corporation
JAGTOME REVOLUTION RX 39-20-260-025 Material Number: M00584240 2 03/11/2022 Boston Scientific Corporation
JAGTOME REVOLUTION RX 39-20-450-025 Material Number: M00584250 2 03/11/2022 Boston Scientific Corporation
JAGTOME REVOLUTION RX 39-30-260-025 Material Number: M00584260 2 03/11/2022 Boston Scientific Corporation
JAGTOME RX 39-20-260-025 Material Number: M00573080 2 03/11/2022 Boston Scientific Corporation
JAGTOME RX 39-20-450-025 Material Number: M00573090 2 03/11/2022 Boston Scientific Corporation
JAGTOME RX 39-30-260-025 Material Number: M00573100 2 03/11/2022 Boston Scientific Corporation
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