Medical Device Recalls
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1 result found
Recall Number: Z-2147-2016 |
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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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| AORTIC ARCH CANNULA, Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass (part numbers NA... | 2 | 07/08/2016 |
FEI # 1718850 Sorin Group USA, Inc. |
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