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U.S. Department of Health and Human Services

Medical Device Recalls
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31 to 34 of 34 Results
510(K) Number: K171957
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Product Description
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Recall
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FDA Recall
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CENTRAL LINE BUNDLE 16CM MULTIMED ECVC6545 2 10/09/2019 Centurion Medical Products Corporation
CENTRAL LINE BUNDLE ECVC6375 2 10/09/2019 Centurion Medical Products Corporation
CAP CHANGE KIT DYNDC1496B 2 10/09/2019 Centurion Medical Products Corporation
CAP BUNDLE KIT DYNDC2137 2 10/09/2019 Centurion Medical Products Corporation
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