Medical Device Recalls
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11 to 20 of 34 Results
510(K) Number: K171957 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
STERILE CAP CHANGE KIT DYNDC1946B | 2 | 10/09/2019 | Centurion Medical Products Corporation |
CAP BUNDLE KIT DYNDC2137 | 2 | 10/09/2019 | Centurion Medical Products Corporation |
TRIPLE LUMEN BUNDLE KIT ECVC1540 | 2 | 10/09/2019 | Centurion Medical Products Corporation |
CENTRAL VENOUS ACCESS DEVICE BUNDLE ECVC2840 | 2 | 10/09/2019 | Centurion Medical Products Corporation |
CVC BUNDLE, 20CM, 4L, PI ECVC5095 | 2 | 10/09/2019 | Centurion Medical Products Corporation |
CVC BUNDLE, 20CM, 3L, PI ECVC5120 | 2 | 10/09/2019 | Centurion Medical Products Corporation |
CVC BUNDLE, 20CM, 3L, PI ECVC5120A | 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 TRIPLE LUMEN SAFETY BUNDLE ECVC6070 | 2 | 10/09/2019 | Centurion Medical Products Corporation |
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