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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 25 of 25 Results
510(K) Number: K112372
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FDA Recall
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Cardiosave Rescue IABP - Product Usage: used to inflate and deflate intra-aortic balloons. It provid... 3 04/28/2021 FEI # 3001418283
Datascope Corp.
Cardiosave Rescue Intra-Aortic Balloon Pump (IABP), Model Numbers 0998-00-0800-75, 0998-00-0800-83, ... 2 03/06/2023 FEI # 3001418283
Datascope Corp.
Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP), Containing Coiled Cord cable (part number 0012-... 1 03/09/2023 FEI # 3001418283
Datascope Corp.
MAQUET CARDIOSAVE hybrid Intra-Aortic Balloon Pump, Model Number 0998-XX-0800-32 2 04/26/2023 FEI # 3001418283
Datascope Corp.
Maquet CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP) 2 02/23/2015 FEI # 3001418283
Maquet Datascope Corp - Cardiac Assist Division
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