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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
Related Medical Device Recalls Recall Date to: 09/17/2014
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Product Description
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Class
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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 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 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 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 Stryker Howmedica Osteonics Corp.
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