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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 17 Results
510(K) Number: K112372
 
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Cardiosave Hybrid IABP - Product Usage: used to inflate and deflate intra-aortic balloons. It provid... 3 04/28/2021 Datascope Corp.
Cardiosave Rescue IABP - Product Usage: used to inflate and deflate intra-aortic balloons. It provid... 3 04/28/2021 Datascope Corp.
Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), Model Nos. 0998-00-0800-31, 0998-00-0800-32, 099... 2 10/07/2021 Datascope Corp.
Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), Model Nos. 0998-00-0800-31, 0998-00-0800-32, 099... 2 09/30/2021 Datascope Corp.
CARDIOSAVE Hybrid IABP and CARDIOSAVE Rescue IABP affected part number is 0998-:XX-0800-XX Li-Ion ... 2 03/02/2017 Maquet Datascope Corp - Cardiac Assist Division
Cardiosave Hybrid and rescue IABP 2 03/25/2016 Maquet Datascope Corp - Cardiac Assist Division
Maquet CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP) 2 02/23/2015 Maquet Datascope Corp - Cardiac Assist Division
CARDIOSAVE Intra-Aortic Balloon Pump and CS300 Intra-Aortic Balloon Pump; and, non-sterile, not for ... 2 02/07/2015 Maquet Datascope Corp - Cardiac Assist Division
CARDIOSAVE Intra-Aortic Balloon Pump An electromechanical system used to inflate and deflate intr... 2 01/09/2013 Maquet Cardiovascular, LLC
Cardiosave Hybrid IntraAortic Balloon Pump. Model UDI 0998-00-0800-31 1060756710... 1 12/30/2021 Datascope Corp.
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