Cardiosave System - Hybrid & Rescue Intra-aortic Balloon Pump (2021-09-14)

CardioSave System Recall Summary The CardioSave System Hybrid and Rescue intra-aortic balloon pump devices are being recalled across Canada due to a medical device issue. These are heart support devices used in hospitals to help patients with severe heart conditions. The recall affects all units of these devices that were distributed in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2021-09-24

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/f8d96e73-874e-40a3-a746-85afaabe7a7d