• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Medical Device Recalls

  • Print
  • Share
  • E-mail
-
21 to 30 of 34 Results
510(K) Number: K171957
 < 
 1 
 2 
 3 
 4 
 > 
Results per Page
New Searchexport reports to excelExport to Excel | HelpHelp
Product Description
Sort by Product Name [A-Z]
Sort by Product Name [Z-A]
Recall
Class
Sort by Recall Class [0-9]
Sort by Recall Class [9-0]
FDA Recall
Posting Date
Sort by Date Classified [0-9]
Sort by Date Classified [9-0]
Recalling Firm
Sort by Recalling Firm [A-Z]
Sort by Recalling Firm [Z-A]
CVC TRIPLE LUMEN SAFETY BUNDLE ECVC6070 2 10/09/2019 Centurion Medical Products Corporation
CVC INSERTION BUNDLE 8.5FR 4L 16CM ECVC6355 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 ECVC5120A 2 10/09/2019 Centurion Medical Products Corporation
CVC BUNDLE, 20CM, 3L, PI ECVC5120 2 10/09/2019 Centurion Medical Products Corporation
CVC BUNDLE WITHOUT CATH CVI4600 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 MULTIMED, 3L, 20CM ECVC6060 2 10/09/2019 Centurion Medical Products Corporation
CENTRAL VENOUS ACCESS DEVICE BUNDLE ECVC2840 2 10/09/2019 Centurion Medical Products Corporation
CENTRAL LINE BUNDLE 16CM MULTIMED ECVC6545A 2 10/09/2019 Centurion Medical Products Corporation
-
-