Heartmate III Lvas Implant Kit (2018-04-05)

HeartMate III LVAS Implant Kit Recall The HeartMate III Left Ventricular Assist System (LVAS) Implant Kit has been recalled across Canada. The recall is classified as Class I, meaning there is a serious risk of adverse health consequences or death. The device is used to help support heart function in patients with heart failure.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2018-05-01
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/46aa9a57-2cfb-4ead-8000-02518e7b74bf