Zenith Alpha Thoracic Endovascular Grafts (2017-06-23)

Zenith Alpha Thoracic Endovascular Grafts Recall Zenith Alpha Thoracic Endovascular Grafts are being recalled across Canada. These are medical devices used to treat certain thoracic aortic conditions. The recall was issued due to concerns with the devices and is classified as a Class I recall, which is the most serious classification.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2017-06-30
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/a0690ed4-c9a8-49d3-9f4a-82a35e5c96d1