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U.S. Department of Health and Human Services

Medical Device Recalls
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41 to 46 of 46 Results
Related Medical Device Recalls
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Z-2461-2011 - Regenerex (TM) Ringloc +, Limited Hole Acetablular Cup, 48 mm Size 22, with Locking Ring, sterile, REF PT-116048, Biomet Orthopedics, Warsaw, IN. Intended Use: The Regenerex Ringloc is intended to... 2 06/08/2011 Biomet, Inc.
Z-2462-2011 - Regenerex (TM) Ringloc +, Limited Hole Acetablular Cup, 50 mm Size 22, with Locking Ring, sterile, REF PT-116050, Biomet Orthopedics, Warsaw, IN. Intended Use: The Regenerex Ringloc is intended to ... 2 06/08/2011 Biomet, Inc.
Z-2463-2011 - Regenerex (TM) Ringloc +, Limited Hole Acetablular Cup, 52 mm Size 23, with Locking Ring, sterile, REF PT-116052, Biomet Orthopedics, Warsaw, IN. Intended Use: The Regenerex Ringloc is intended to r... 2 06/08/2011 Biomet, Inc.
Z-2464-2011 - Regenerex (TM) Ringloc +, Limited Hole Acetablular Cup, 54 mm Size 23, with Locking Ring, sterile, REF PT-116054, Biomet Orthopedics, Warsaw, IN. Intended Use: The Regenerex Ringloc is intended to... 2 06/08/2011 Biomet, Inc.
Z-2465-2011 - Regenerex (TM) Ringloc +, Limited Hole Acetablular Cup, 56 mm Size 24, with Locking Ring, sterile, REF PT-116056, Biomet Orthopedics, Warsaw, IN. Intended Use: The Regenerex Ringloc is intended to... 2 06/08/2011 Biomet, Inc.
Z-2422-2011 - Ringloc + Acetabular Shell limited hole finned 48 mm Size 22 porous coat, for uncemented use, sterile, REF 16-104148, Biomet Orthopedics, Warsaw, IN. Intended Use: The Porous Plasma Spray (PPS) Rin... 2 06/08/2011 Biomet, Inc.
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