Brand
Datascope Corp.: official recall notices
14 official recall or safety notices published on this site name Datascope Corp., dated between 2023-06-05 and 2026-02-06. They were issued by 1 authority: US FDA — Medical Devices (14).
Countries where the notices were issued: United States (14).
Name as written in the notices: Datascope Corp.. This is the brand or the responsible company as each authority recorded it. A recall shows a safety system working; it is not a verdict on a brand. Follow the official notice for each product.
What this page counts: the notices published as pages on product-guru.org, over every date (this site publishes a selection of the notices in the ProductGuru index). The brand scorecards count every indexed notice in a rolling 24-month window instead, so their totals differ from this page.
Notices by year
| Year | Notices |
|---|
| 2026 | 1 |
| 2024 | 3 |
| 2023 | 10 |
Notices by authority
| Authority | Notices |
|---|
| US FDA — Medical Devices | 14 |
All notices
| Date | Authority | Product | Hazard (as classified) |
|---|
| 2026-02-06 | US FDA — Medical Devices | Battery Charging Station; Model: 0998-00-0802; | — |
| 2024-08-08 | US FDA — Medical Devices | CARDIOSAVE HYBRID INTRA-AORTIC BALLOON PUMP (IABP). Electromechanical system used to inflate and deflate intra-aortic ba | — |
| 2024-08-08 | US FDA — Medical Devices | CARDIOSAVE RESCUE INTRA-AORTIC BALLOON PUMP (IABP). Electromechanical system used to inflate and deflate intra-aortic ba | — |
| 2024-08-08 | US FDA — Medical Devices | CARDIOSAVE RESCUE INTRA-AORTIC BALLOON PUMP (IABP). Electromechanical system used to inflate and deflate intra-aortic ba | — |
| 2023-07-31 | US FDA — Medical Devices | Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-31, 0998-UC-0800-31, 0998-00-0800-32, 099 | — |
| 2023-07-31 | US FDA — Medical Devices | Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-31, 0998-UC-0800-31, 0998-00-0800-32, 099 | — |
| 2023-07-31 | US FDA — Medical Devices | Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85 | — |
| 2023-06-23 | US FDA — Medical Devices | LINEAR 7.5Fr.IAB, Intra-Aortic Balloon Catheter and Accessories, used to provide counter pulsation therapy in the aorta | — |
| 2023-06-23 | US FDA — Medical Devices | SENSATION 7 Fr. IAB, Intra-Aortic Balloon Catheter and Accessories, used to provide counter pulsation therapy in the aor | — |
| 2023-06-23 | US FDA — Medical Devices | YAMATO PLUS IAB; intra-aortic balloon catheter and accessories used to provide counter pulsation therapy in the aorta. | — |
| 2023-06-23 | US FDA — Medical Devices | SENSATION PLUS 7.5Fr IAB, Intra-Aortic Balloon Catheter and Accessories, used to provide counter pulsation therapy in th | — |
| 2023-06-23 | US FDA — Medical Devices | TRANS-RAY IAB, Intra-Aortic Balloon Catheter and Accessories, used to provide counter pulsation therapy in the aorta | — |
| 2023-06-05 | US FDA — Medical Devices | Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), Model numbers 0998-00-0800-31 0998-00-0800-32 0998-00-0800-33 0 | — |
| 2023-06-05 | US FDA — Medical Devices | Cardiosave Rescue Intra-Aortic Balloon Pump (IABP), Model numbers 0998-00-0800-75 0998-00-0800-83 0998-00-0800-85 | — |
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