Cardiosave System - Hybrid & Rescue Intra-aortic Balloon Pump
Cardiosave System Recall Summary The Cardiosave System Hybrid & Rescue Intra-Aortic Balloon Pump is being recalled in Canada due to a performance issue. This device is used to support heart function in certain medical patients. The recall affects units distributed across 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
- 2023-01-04
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/5b839a55-c48a-4ca2-89d2-0a34488c0537