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 4 of 4 Results
510(K) Number: K031623
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]
Medtronic U-CLIP Double Arm Approximation Device, model V100D U-Clip, Catalog Number V100DRFRN2. St... 2 07/17/2010 Medtronic Cardiovascular Revascularization & Surgical Therap
VNUS Medical U-CLIP Removal Tool, UREM1860, is intended for the removal of U-Clip anastomotic device... 2 09/16/2008 Medtronic Cardiac Surgery Technologies
Medtronic U-CLIP Anastomotic Device Removal Tool, model REM1860FW. The U-Clip Anastomotic Device Re... 2 06/27/2007 Medtronic Cardiac Surgery Technologies
Medtronic SPYDER Anastomotic Device. Sterilized using irradiation. Do not Reuse. Nonpyrogenic. T... 2 04/13/2006 Medtronic Cardiac Surgery Technologies
-
-