Medical Device Recalls
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1 result found
510(K) Number: K033323 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| D 903 Avant Oxygenator extracorporeal membrane, Sterile EO, Distributed in U.S. by: Sorin Group USA,... | 2 | 01/14/2012 |
FEI # 1718850 Sorin Group USA, Inc. |
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