Relay®pro Thoracic Stent-graft System

Relay Pro Thoracic Stent-Graft System Recall The Relay Pro Thoracic Stent-Graft System is being recalled in Canada due to a device performance issue. This stent-graft system is used in thoracic (chest) aorta procedures. The recall affects all units distributed across Canada and has been classified as a Class I recall, indicating a serious potential health risk.

Product

Relay®Pro Thoracic Stent-Graft System

Reason

Device performance issue

Classification

Class I

Category

medical device recall

Country

Canada

Agency

HC-DEVICES

Recall date

2026-05-29

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/36944e16-e0eb-4246-8973-2a2371301a46