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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 15 of 15 Results
Related Medical Device Recalls Recall Date to: 06/10/2014
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Product Description
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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.
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