Medical Device Recalls
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1 result found
510(K) Number: K790246 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| CPB Catheter Kit Product Usage: Venous Return Cannula is indicated for venous drainage during ca... | 2 | 07/23/2014 |
FEI # 1828100 Terumo Cardiovascular Systems Corporation |
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