Medical Device Recalls
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1 result found
Recall Number: Z-2838-2020 |
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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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| Datascope Intra-Aortic Ballon Catheters (IABs)-Linear 7.5Fr 25cc IAB Kit P/N: 0684-00-0478-01, 068... | 2 | 08/21/2020 |
FEI # 1000222374 Datascope Corporation |
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