Cardiosave System - Hybrid & Rescue Intra-aortic Balloon Pump (2016-04-05)
CardioSave System Intra-Aortic Balloon Pump Recall The CardioSave System Hybrid and Rescue intra-aortic balloon pumps are being recalled across Canada. These medical devices are used to help support heart function during cardiac procedures or emergencies. The recall was issued due to a device safety concern, though specific technical details are not provided in this notice.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2016-04-22
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/f93ae2b9-e3a1-41f4-8622-15fa17fa3a61