Medical Device Recalls
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Related Medical Device Recalls |
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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| Z-1939-2019 - Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), 0998-00-0800-53 For cardiovascular use. | 1 | 07/16/2019 | Datascope Corp. |
| Z-1940-2019 - Cardiosave Rescue IABP, 0998-00-0800-83 Intra-Aortic Balloon Pump For cardiovascular use. | 1 | 07/16/2019 | Datascope Corp. |
| Z-1944-2019 - CS300 Intra-Aortic Balloon Pump, English, 220V; 0998-00-3023-55 For cardiovascular use. | 1 | 07/16/2019 | Datascope Corp. |
| Z-1942-2019 - CS100 Intra-Aortic Balloon Pump, English, 220V; 0998-00-3013-55 For cardiovascular use. | 1 | 07/16/2019 | Datascope Corp. |
| Z-1943-2019 - CS300 Intra-Aortic Balloon Pump, English, 110V; 0998-00-3023-53 For cardiovascular use. | 1 | 07/16/2019 | Datascope Corp. |
| Z-1941-2019 - CS100 Intra-Aortic Balloon Pump, English, 110V; 0998-00-3013-53 For cardiovascular use. | 1 | 07/16/2019 | Datascope Corp. |
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