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 Hybrid IntraAortic Balloon Pump. Model UDI 0998-00-0800-31 1060756710... | 1 | 12/30/2021 | Datascope Corp. |
Cardiosave Li-Ion Battery Pack, Part No. 0146-00-0097. Component of the Cardiosave Hybrid Intra-Aor... | 1 | 10/20/2021 | Datascope Corp. |
CS100 Intra-Aortic Balloon Pump, English, 110V; 0998-00-3013-53 For cardiovascular use. | 1 | 07/16/2019 | Datascope Corp. |
CS100 Intra-Aortic Balloon Pump, English, 220V; 0998-00-3013-55 For cardiovascular use. | 1 | 07/16/2019 | Datascope Corp. |
Cardiosave Rescue IABP, 0998-00-0800-83 Intra-Aortic Balloon Pump For cardiovascular use. | 1 | 07/16/2019 | Datascope Corp. |
Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), 0998-00-0800-53 For cardiovascular use. | 1 | 07/16/2019 | Datascope Corp. |
CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP), Part Number 0998-00-0800-XX & 0998-UC-0800-XX (e... | 1 | 05/31/2018 | Maquet Datascope Corp - Cardiac Assist Division |
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