Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K081124 |
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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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Modular SMF(TM) The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems are indicated for individual... | 2 | 01/04/2017 | Smith & Nephew, Inc. |
12/14 TAPER HIGH OFFSET NECK USE WITH SMITH & NEPHEW STEMS AND 12/14 FEMORAL COMPONENTS ONLY CO-CR, ... | 2 | 09/20/2012 | Smith & Nephew Inc |
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