Medical Device Recalls
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1 result found
510(K) Number: K150862 |
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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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ACTIS Flex Reamers SZ 0/1; 2/3; 4/5; 6/7; 8/9; 10/11; 12, Product is sold non-sterile, these instrum... | 2 | 11/21/2016 | Depuy Orthopaedics Inc. |
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