Medical Device Recalls
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1 result found
510(K) Number: K052081 |
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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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FlexFlow Venous Cannula Model/Catalog Number 200-200 The FlexFlow Venous Cannula is a single use st... | 2 | 11/08/2017 | Sorin Group USA, Inc. |
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