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U.S. Department of Health and Human Services

Medical Device Recalls

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11 to 20 of 30 Results
Recall Date to: 04%2F20%2F2014 510(K) Number: K093235
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Product Description
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Ringloc + Acetabular Shell limited hole finned 70 mm Size 28 porous coat, for uncemented use, steril... 2 06/08/2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole, 46 mm Size 22 porous coat, for uncemented use, sterile, REF... 2 06/08/2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole, 48 mm Size 22, porous coat, for uncemented use, sterile, RE... 2 06/08/2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole, 50 mm Size 23, porous coat, for uncemented use, sterile, RE... 2 06/08/2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole, 52 mm Size 23, porous coat, for uncemented use, sterile, RE... 2 06/08/2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole, 54 mm Size 24, porous coat, for uncemented use, sterile, RE... 2 06/08/2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole, 56 mm Size 24, porous coat, for uncemented use, sterile, RE... 2 06/08/2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole, 58 mm Size 25, porous coat, for uncemented use, sterile, RE... 2 06/08/2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole, 60 mm Size 25, porous coat, for uncemented use, sterile, RE... 2 06/08/2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole, 62 mm Size 26, porous coat, for uncemented use, sterile, RE... 2 06/08/2011 Biomet, Inc.
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