Cardiosave Hybrid And Rescue Intra-aortic Balloon Pump

Recall Summary Cardiosave Hybrid and Rescue intra-aortic balloon pumps (devices used to support heart function) are being recalled across Canada because they may not function as intended due to a manufacturing defect. The devices are used in hospitals to help patients with failing hearts. This recall affects all units of these two models distributed in Canada.

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-01-25

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/fe520756-38d8-4d2e-af9a-6125ebc59a2e