Cardiosave System - Hybrid & Rescue Intra-aortic Balloon Pump (2015-12-21)

CardioSave System Recall Summary The CardioSave System Hybrid & Rescue intra-aortic balloon pump is being recalled across Canada. This is a Class I recall, meaning there is a serious potential health risk associated with the device. The recall applies to all units distributed in Canada as of the recall date in December 2015.

Reason

Health products

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-01-22

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/5b9ac1ba-1074-48f9-a32b-c44aa01e6d17