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U.S. Department of Health and Human Services

Medical Device Recalls

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21 to 30 of 34 Results
510(K) Number: K171957
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Product Description
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FDA Recall
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CVC INSERTION BUNDLE 8.5FR 4L 16CM ECVC6355 2 10/09/2019 Centurion Medical Products Corporation
CENTRAL LINE BUNDLE ECVC6375 2 10/09/2019 Centurion Medical Products Corporation
CENTRAL LINE BUNDLE 16CM MULTIMED ECVC6545 2 10/09/2019 Centurion Medical Products Corporation
CENTRAL LINE BUNDLE 16CM MULTIMED ECVC6545A 2 10/09/2019 Centurion Medical Products Corporation
OR VANTEX 7FR 3L 16CM CVC ECVC6665 2 10/09/2019 Centurion Medical Products Corporation
VANTEX 7FR, 16CM, 3L CVC BUNDLE ECVC6670 2 10/09/2019 Centurion Medical Products Corporation
IV START KIT IV8440 2 10/09/2019 Centurion Medical Products Corporation
IV SECUREMENT KIT IVS3405 2 10/09/2019 Centurion Medical Products Corporation
IV KIT - SORBAVIEW IVS3475 2 10/09/2019 Centurion Medical Products Corporation
INVASIVE PROCEDURE TRAY MNS9510 2 10/09/2019 Centurion Medical Products Corporation
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