Medical Device Recalls
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1 result found
510(K) Number: K012952 |
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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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Hemashield Gold Woven Double Velour Vascular Branch Graft | 2 | 07/22/2010 | Maquet Cardiovascular, LLC |
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