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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 32 Results
510(K) Number: K181122
 
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CARDIOSAVE HYBRID INTRA-AORTIC BALLOON PUMP (IABP). Electromechanical system used to inflate and def... 1 09/20/2024 FEI # 3001418283
Datascope Corp.
CARDIOSAVE HYBRID INTRA-AORTIC BALLOON PUMP (IABP). Electromechanical system used to inflate and def... 1 09/20/2024 FEI # 3001418283
Datascope Corp.
CARDIOSAVE RESCUE INTRA-AORTIC BALLOON PUMP (IABP). Electromechanical system used to inflate and def... 1 09/20/2024 FEI # 3001418283
Datascope Corp.
CARDIOSAVE RESCUE INTRA-AORTIC BALLOON PUMP (IABP). Electromechanical system used to inflate and def... 1 09/20/2024 FEI # 3001418283
Datascope Corp.
CS100 Intra-Aortic Balloon Pump, English, 110V; 0998-00-3013-53 For cardiovascular use. 1 07/16/2019 FEI # 3001418283
Datascope Corp.
CS100 Intra-Aortic Balloon Pump, English, 220V; 0998-00-3013-55 For cardiovascular use. 1 07/16/2019 FEI # 3001418283
Datascope Corp.
Cardiosave Hybrid Model Nos. 0998-00-0800-31 0998-00-0800-32 0998-00-0800-33 0998-00-0800-34 ... 1 03/09/2023 FEI # 3001418283
Datascope Corp.
Cardiosave Hybrid IABP, Part Number 0998-00-0800-53 1 10/27/2018 FEI # 3001418283
Maquet Datascope Corp - Cardiac Assist Division
Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), 0998-00-0800-53 For cardiovascular use. 1 07/16/2019 FEI # 3001418283
Datascope Corp.
Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), Model Numbers 0998-00-0800-31, 0998-00-0800-32, ... 1 01/19/2023 FEI # 3001418283
Datascope Corp.
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