Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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
-
1 to 3 of 3 Results
PMA Number: P930038
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]
Angio-Seal Vascular Closure Device. Ref 610109. 6F STS Platform. Sterilized by gamma radiation. ... 2 03/25/2006 St. Jude Medical / Daig Division
The affected device is labeled Angio-Seal Vascular Closure Device 6F VIP Platform, model 610130. Th... 3 11/07/2006 St. Jude Medical / Daig Division
Angio-Seal Evolution Vascular Closure Device, Cat. No. C610135 2 06/29/2018 Terumo Medical Corp
-
-