• 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 2 of 2 Results
Related Medical Device Recalls Date Classified to: 07/29/2014
Results per Page
New SearchExport all 2 Records 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]
Date
Posted
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]
Z-1691-2008 - X-Celerate Universal Block Pegless Size #3, Non Sterile; 2 Sep-20-2008 Stryker Howmedica Osteonics Corp.
Z-1690-2008 - Universal Notch Preparation Guide, Size #3; Non Sterile; Howmedica Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430; authorized representative in Europe: Stryker France ZAC Satolas Green Pus... 2 Sep-20-2008 Stryker Howmedica Osteonics Corp.
-
-