Zenith Alpha Abdominal Endovascular Graft (2020-08-11)

Zenith Alpha Abdominal Endovascular Graft Recall Zenith Alpha Abdominal Endovascular Grafts are being recalled in Canada due to a device defect. These grafts are used in surgical procedures to treat abdominal aortic aneurysms. The recall affects devices distributed across Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2020-08-28
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/1581bf39-93ef-4b7b-a9c3-fba2ebb0fca8