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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: 07/04/2015 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 finned 48 mm Size 22 porous coat, for uncemented use, steril... 2 06/08/2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole finned 50 mm Size 23 porous coat, for uncemented use, steril... 2 06/08/2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole finned 52 mm Size 23 porous coat, for uncemented use, steril... 2 06/08/2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole finned 54 mm Size 24 porous coat, for uncemented use, steril... 2 06/08/2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole finned 56 mm Size 24 porous coat, for uncemented use, steril... 2 06/08/2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole finned 58 mm Size 25 porous coat, for uncemented use, steril... 2 06/08/2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole finned 60 mm Size 25 porous coat, for uncemented use, steril... 2 06/08/2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole finned 62 mm Size 26 porous coat, for uncemented use, steril... 2 06/08/2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole finned 64 mm Size 26 porous coat, for uncemented use, steril... 2 06/08/2011 Biomet, Inc.
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