• 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 5 of 5 Results
510(K) Number: K023528
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]
Zimmer Natural-Knee II System Modular Cemented Tibial Baseplate, Right, Size 00, for cemented use on... 2 06/30/2009 Zimmer Inc.
Zimmer Natural-Knee II System Modular Cemented Tibial Baseplate, Left, Size 00, for cemented use onl... 2 06/30/2009 Zimmer Inc.
Zimmer Natural-Knee II System Modular Cemented Tibial Baseplate, Right, Size 0, TIB B/PL, for cement... 2 06/30/2009 Zimmer Inc.
Zimmer Natural-Knee II System Modular Cemented Tibial Baseplate, Left, Size 0, TIB B/PL, for cemente... 2 06/30/2009 Zimmer Inc.
Zimmer Natural-Knee II System Modular Cemented Tibial Baseplate, Right, Size 3, For cemented use onl... 2 01/09/2009 Zimmer Inc.
-
-