• 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
-
11 to 15 of 15 Results
Related Medical Device Recalls
 < 
 1 
 2 
 
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]
Z-0898-2009 - Omnifit FC Cemented Stem These devices are modular components of a total hip system. These femoral stems are intended for use with femoral heads and acetabular components in primary or revision tot... 2 01/26/2009 Stryker Howmedica Osteonics Corp.
Z-0899-2009 - Omnifit Eon These devices are modular components of a total hip system. These femoral stems are intended for use with femoral heads and acetabular components in primary or revision total hip arthro... 2 01/26/2009 Stryker Howmedica Osteonics Corp.
Z-0900-2009 - Japanese Omnifit Eon 127 NK These devices are modular components of a total hip system. These femoral stems are intended for use with femoral heads and acetabular components in primary or revision ... 2 01/26/2009 Stryker Howmedica Osteonics Corp.
Z-0901-2009 - Reunion HA Fracture Stem These devices are modular components of a total hip system. These femoral stems are intended for use with femoral heads and acetabular components in primary or revision tot... 2 01/26/2009 Stryker Howmedica Osteonics Corp.
Z-0889-2009 - Triathlon Cemented Stem - Knee These devices are modular components of a total knee system. These modular stems are intended for use with femoral and tibial components in primary or revision total ... 2 01/26/2009 Stryker Howmedica Osteonics Corp.
-
-