Medical Device Recalls
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11 to 13 of 13 Results
510(K) Number: K040770 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Biomet Series A Standard Patella size 25mm, one peg, Part 184700, Sterile, Biomet Orthopedics, Wars... | 2 | 01/11/2012 | Biomet, Inc. |
Biomet Series A Thin Patella size 25mm, three pegs, Part 184780, Sterile, Biomet Orthopedics, Warsaw... | 2 | 01/11/2012 | Biomet, Inc. |
Biomet Series A Thin Patella size 25mm, one peg - 184720, Sterile, Biomet Orthopedics, Warsaw, IN 46... | 2 | 01/11/2012 | Biomet, Inc. |
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