Medical Device Recalls
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11 to 15 of 15 Results
510(K) Number: K953337 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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Por fullct fem st 17x200mm, Sterile, | 2 | 03/20/2017 | Zimmer Biomet, Inc. |
Por fullct fem st 16x200mm, Sterile, | 2 | 03/20/2017 | Zimmer Biomet, Inc. |
Por fullct fem st 15x200mm, Sterile, prosthesis, hip, semi-constrained, metal/polymer, porous unce... | 2 | 03/20/2017 | Zimmer Biomet, Inc. |
6 DEGREE COCR FEM HEAD 36 | 2 | 02/20/2014 | Zimmer, Inc. |
12/14 COCR FEMORAL HEAD (2, 3 and 4); 12/14 FEMORAL HEAD (+7X28M and 7X32M) | 2 | 02/20/2014 | Zimmer, Inc. |
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