Medical Device Recalls
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21 to 27 of 27 Results
Recall Date to: 11/26/2014 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, 62 mm Size 26, 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, 66 mm Size 27, 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, 70 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 finned 48 mm Size 22 porous coat, for uncemented use, steril... | 2 | 06/08/2011 | Biomet, Inc. |
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