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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 27 of 27 Results
510(K) Number: K112372
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Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), 0998-00-0800-53 For cardiovascular use. 1 07/16/2019 Datascope Corp.
CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP), Part Number 0998-00-0800-XX & 0998-UC-0800-XX (e... 1 05/31/2018 Maquet Datascope Corp - Cardiac Assist Division
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
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