Cardiosave System - Hybrid & Rescue Intra-aortic Balloon Pump
Recall Summary Cardiosave System Hybrid and Rescue Intra-Aortic Balloon Pumps are being recalled across Canada due to a performance issue. These are medical devices used to support heart function in certain patients. The recall affects all units of these devices that were 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
- 2023-03-16
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/744d4934-cc2c-4c6a-842b-654d2cef8111