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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 28 Results
Recall Date to: 03/27/2015 510(K) Number: K093235
 
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Ringloc+ Acetabular Shell Finned 52 mm, PN 16-104152, hip prosthesis component. 2 02/17/2015 Biomet, Inc.
Ringloc + Acetabular Shell limited hole, 76 mm Size 28, porous coat, for uncemented use, sterile, RE... 2 06/08/2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole, 72 mm Size 28, porous coat, for uncemented use, sterile, RE... 2 06/08/2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole, 70 mm Size 28, porous coat, for uncemented use, sterile, RE... 2 06/08/2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole, 68 mm Size 27, porous coat, for uncemented use, sterile, RE... 2 06/08/2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole, 66 mm Size 27, porous coat, for uncemented use, sterile, RE... 2 06/08/2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole, 64 mm Size 26, 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.
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, 58 mm Size 25, porous coat, for uncemented use, sterile, RE... 2 06/08/2011 Biomet, Inc.
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