Medical Device Recalls
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1 result found
510(K) Number: K121563 |
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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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Corin TriFit TS, Size 8, Standard Tapered Stem, REF 694.0008, Sterile. | 2 | 09/30/2021 | Corin Ltd |
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