Medical Device Recalls
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21 to 27 of 27 Results
Recall Date to: 10/24/2014 510(K) Number: K093235 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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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 56 mm Size 24 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 52 mm Size 23 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 48 mm Size 22 porous coat, for uncemented use, steril... | 2 | 06/08/2011 | Biomet, Inc. |
Ringloc + Acetabular Shell limited hole finned 46 mm Size 22 porous coat, for uncemented use, steril... | 2 | 06/08/2011 | Biomet, Inc. |
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