Medical Device Recalls
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21 to 27 of 27 Results
510(K) Number: K112372 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
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 Intra-Aortic Balloon Pumps (IABP), Model Number 0998-00-0800-55, Part Number 0998-... | 3 | 06/14/2023 | Datascope Corp. |
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. |
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