Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K071723 |
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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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Fitmore" Hip Stem | 2 | 11/06/2012 | Zimmer, Inc. |
Fitmore Hip Stem, hip prosthesis, various sizes, Item Nos. 0100551102 0100551103 0100551104 01005... | 2 | 11/07/2019 | Zimmer Biomet, Inc. |
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