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U.S. Department of Health and Human Services

Medical Device Recalls
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Related Medical Device Recalls
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Product Description
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Z-1681-2011 - SCORPIO CR TIBIAL TRIAL, non sterile, made in the USA Howmedica Osteonics Corp., 325 Corporate Drive, Mahwah, NJ 07430. The Tibial trial are utilized during surgery to assess the overall componen... 2 03/16/2011 FEI # 3003070421
Stryker Howmedica Osteonics Corp.
Z-1682-2011 - SCORPIO PS TIBIAL TRIAL, non sterile, made in the USA Howmedica Osteonics Corp., 325 Corporate Drive, Mahwah, NJ 07430. The Tibial trial are utilized during surgery to assess the overall componen... 2 03/16/2011 FEI # 3003070421
Stryker Howmedica Osteonics Corp.
Z-1684-2011 - SCORPIO-FLEX CR TIBIAL TRIAL, non sterile, made in the USA Howmedica Osteonics Corp., 325 Corporate Drive, Mahwah, NJ 07430. The Tibial trial are utilized during surgery to assess the overall compo... 2 03/16/2011 FEI # 3003070421
Stryker Howmedica Osteonics Corp.
Z-1683-2011 - SCORPIO-FLEX PS TIBIAL TRIAL, non sterile, made in the USA Howmedica Osteonics Corp., 325 Corporate Drive, Mahwah, NJ 07430. The Tibial trial are utilized during surgery to assess the overall com... 2 03/16/2011 FEI # 3003070421
Stryker Howmedica Osteonics Corp.
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