Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K003836 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Synthes USA, TI Synex (TM) II Central Body 37mm - 52mm, Catalog number 04.808.006. Intended for u... | 1 | 11/09/2009 | Synthes USA (HQ), Inc. |
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