Medical Device Recalls
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21 to 27 of 27 Results
510(K) Number: K112372 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Cardiosave Rescue IABP - Product Usage: used to inflate and deflate intra-aortic balloons. It provid... | 3 | 04/28/2021 | Datascope Corp. |
Cardiosave Rescue IABP, 0998-00-0800-83 Intra-Aortic Balloon Pump For cardiovascular use. | 1 | 07/16/2019 | Datascope Corp. |
Cardiosave Rescue Intra-Aortic Balloon Pump (IABP), Model Numbers 0998-00-0800-75, 0998-00-0800-83, ... | 2 | 03/06/2023 | Datascope Corp. |
Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP), Containing Coiled Cord cable (part number 0012-... | 1 | 03/09/2023 | Datascope Corp. |
Cardiosave Rescue IntraAortic Balloon Pump. Model UDI 0998-00-0800-75 1060756711... | 1 | 12/30/2021 | Datascope Corp. |
MAQUET CARDIOSAVE hybrid Intra-Aortic Balloon Pump, Model Number 0998-XX-0800-32 | 2 | 04/26/2023 | Datascope Corp. |
Maquet CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP) | 2 | 02/23/2015 | Maquet Datascope Corp - Cardiac Assist Division |
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