Medical Device Recalls
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1 to 10 of 34 Results
510(K) Number: K171957 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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CAP BUNDLE KIT DYNDC2137 | 2 | 10/09/2019 | Centurion Medical Products Corporation |
CAP CHANGE KIT DYNDC1496B | 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 |
CENTRAL VENOUS ACCESS DEVICE BUNDLE ECVC2840 | 2 | 10/09/2019 | Centurion Medical Products Corporation |
CVC BUNDLE MULTIMED, 3L, 20CM ECVC6060 | 2 | 10/09/2019 | Centurion Medical Products Corporation |
CVC BUNDLE VANTEX 7F, 3L, 20CM ECVC6065 | 2 | 10/09/2019 | Centurion Medical Products Corporation |
CVC BUNDLE WITHOUT CATH CVI4600 | 2 | 10/09/2019 | Centurion Medical Products Corporation |
CVC BUNDLE, 20CM, 3L, PI ECVC5120 | 2 | 10/09/2019 | Centurion Medical Products Corporation |
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