Medical Device Recalls
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1 result found
510(K) Number: K112779 |
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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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APEX INTERFACE Hemi 54X and Flared 56X, 3 Hole Acetabular Shells; Model: H5-12354, H5-11356. Pr... | 2 | 08/21/2015 | Omnilife Science Inc. |
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