Medical Device Recalls
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1 result found
Recall Date to: 04/25/2015 510(K) Number: K063251 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Zimmer Kinectivo Technology Modular Neck, BB, 12/14 neck taper, sterile, Zimmer, Warsaw, IN; Catalog... | 2 | 07/27/2009 | Zimmer Inc. |
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