• 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: K083772
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]
Aesculap Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5-F7 2 12/13/2013 Aesculap, Inc.
COLUMBUS REV F TIBIA OFFSET CEMENTED, Knee implant components, various sizes, model nos. NR068K NR... 2 03/13/2020 Aesculap Implant Systems LLC
Columbus Revision Knee System, EnduRo Knee System Product Usage: The Columbus Revision Knee Syst... 2 03/03/2016 Aesculap, Inc.
Columbus Tibia Plateau (component of the Columbus REVISION Knee System) Product Usage - The Colum... 2 06/26/2015 Aesculap Implant Systems
-
-