Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K151254 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| CS300 Intra-Aortic Balloon Pump, English, 110V; 0998-00-3023-53 For cardiovascular use. | 1 | 07/16/2019 |
FEI # 3001418283 Datascope Corp. |
| CS300 Intra-Aortic Balloon Pump, English, 220V; 0998-00-3023-55 For cardiovascular use. | 1 | 07/16/2019 |
FEI # 3001418283 Datascope Corp. |
| CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP), Part Number 0998-00-0800-XX & 0998-UC-0800-XX (e... | 1 | 05/31/2018 |
FEI # 3001418283 Maquet Datascope Corp - Cardiac Assist Division |
| CS 300 Intra-Aortic Balloon Pump. It supports the heart's left ventricle by increasing coronary p... | 1 | 09/05/2017 |
FEI # 3001418283 Maquet Datascope Corp - Cardiac Assist Division |
| CS 300 Intra-Aortic Balloon Pump | 1 | 06/23/2017 |
FEI # 3001418283 Maquet Datascope Corp - Cardiac Assist Division |
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