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 Intra-Aortic Balloon Pumps (IABP), Containing Coiled Cord cable (part number 0012-... | 1 | 03/09/2023 | Datascope Corp. |
Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), Model Numbers 0998-00-0800-31, 0998-00-0800-32, ... | 2 | 03/22/2023 | Datascope Corp. |
Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), Model Numbers Model Numbers 0998-00-0800-75, 099... | 2 | 03/22/2023 | Datascope Corp. |
Cardiosave Intra-Aortic Balloon Pump (IABP) Safety Disk, Model Number 0202-00-0140 | 2 | 03/22/2023 | Datascope Corp. |
Cardiosave Intra-Aortic Balloon Pump (IABP) Pneumatic Interface Module (PIM) , Model Number 0997-00-... | 2 | 03/22/2023 | Datascope Corp. |
MAQUET CARDIOSAVE hybrid Intra-Aortic Balloon Pump, Model Number 0998-XX-0800-32 | 2 | 04/26/2023 | Datascope Corp. |
Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Model Number 0998-00-0800-55, Part Number 0998-... | 3 | 06/14/2023 | Datascope Corp. |
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