• 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: K923277
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]
FOUNDATION KNEE SYSTEM Tibial Fixed Impactor, Revision A and B; Catalog #801-01-449; distributed by ... 2 09/29/2008 Encore Medical, Lp
Size 6 right Foundation Total Knee System (Catalog #324-01-106) knee joint replacement. 2 12/29/2005 Encore Medical, Lp
Foundation Knee System, Tibia-Nonporous, Size 6, Right, sterile. Manufactured by Encore Orthopeadic... 3 07/20/2004 Encore Medical, LP
Foundation Knee System, non-porous Femur Size 8, Right 2 07/30/2003 Encore Medical, LP
-
-