Medical Device Recalls
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31 to 33 of 33 Results
510(K) Number: K181122 |
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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| Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), 0998-00-0800-53 For cardiovascular use. | 1 | 07/16/2019 | Datascope Corp. |
| Cardiosave Rescue IABP, Part Number 0998-UC-0800-83 | 1 | 10/27/2018 | Maquet Datascope Corp - Cardiac Assist Division |
| Cardiosave Hybrid IABP, Part Number 0998-00-0800-53 | 1 | 10/27/2018 | Maquet Datascope Corp - Cardiac Assist Division |
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