Allura Xper Fd10

Allura Xper FD10 Recall Summary The Allura Xper FD10 medical device is being recalled across Canada due to a device performance issue. This is a Class II recall, which means the device may not function as intended but poses limited risk. The recall affects all units of this device that were distributed throughout Canada.

Product

Allura Xper FD10

Reason

Device performance issue

Classification

Class II

Category

medical device recall

Country

Canada

Agency

HC-DEVICES

Recall date

2026-07-08

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/1a6a175c-138b-49b6-960a-da2ec82f7e2b