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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
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Z-1675-2010 - Mallory Head Calcar Femoral 55 mm resection/porous coated 15.0 mm x 220 mm left stem, Sterile, REF 11-104972, Biomet Orthopaedics, Warsaw, IN. Implant device intended for use in femoral revisio... 2 05/26/2010 Biomet, Inc.
Z-1676-2010 - 17 mm Mallory Head Calcar 45 mm repl. fmrl. /100% porous 18.5 mm minimum ream dia x 260 mm rt., Sterile, REF CP154591, Biomet Orthopaedics, Warsaw, IN. Implant device intended for use in femora... 2 05/26/2010 Biomet, Inc.
Z-1677-2010 - 17 mm Mallory Head Calcar 55 mm repl. femoral/100% porous 18.5 mm minimum ream dia. x 220 mm rt., Sterile, REF CP154593, Biomet Orthopaedics, Warsaw, IN. Implant device intended for use in fem... 2 05/26/2010 Biomet, Inc.
Z-1678-2010 - 19 mm Mallory Head Calcar 45 mm repl. femoral/100% porous 20.5 mm minimum ream dia. x 260 mm rt., Sterile, REF CP154599, Biomet Orthopaedics, Warsaw, IN. Implant device intended for use in fem... 2 05/26/2010 Biomet, Inc.
Z-1666-2010 - Mallory Head Calcar Provisional, 45 mm replacement stem, 13.0 x 220 mm left, Sterile, REF 104986, Biomet Orthopaedics, Warsaw, IN. Implant device intended for use in femoral revision surgery. 2 05/26/2010 Biomet, Inc.
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