Zenith Alpha Abdominal Endovascular Graft (2019-04-25)

Zenith Alpha Abdominal Endovascular Graft Recall Zenith Alpha Abdominal Endovascular Grafts have been recalled in Canada due to a defect in the medical device. This graft is an implanted device used to treat abdominal aortic aneurysms. The recall affects all units distributed across Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2019-04-30
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/7c9abec1-6601-45e7-92b0-3dbd9c9357ea