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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
Recall Number: Z-2833-2020
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Datascope Intra-Aortic Ballon Catheters (IABs)-MEGA 8Fr 50cc IAB Kit P/N: 0684-00-0296-01, 0684-00-0... 2 08/21/2020 FEI # 1000222374
Datascope Corporation
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