Cardiosave System - Hybrid & Rescue Intra-aortic Balloon Pump
Recall Summary The Cardiosave System - Hybrid & Rescue Intra-Aortic Balloon Pump is being recalled across Canada due to a performance issue. This device is used to support heart function in certain patients. The recall affects all units distributed in Canada.
- Product
- Cardiosave System - Hybrid & Rescue Intra-Aortic Balloon Pump
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2023-02-17
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/3a6226b7-3ca1-4283-9c2c-c10ae761c72e