Zenith Alpha Abdominal Endovascular Graft (2018-09-17)

Zenith Alpha Abdominal Endovascular Graft Recall Zenith Alpha Abdominal Endovascular Grafts are being recalled in Canada due to safety concerns with the medical device. This graft is used in surgical procedures 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

2018-10-05

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/7b04a83b-2ed2-483c-8622-f89c3acbf8f2