Wendylett 4way

WendyLett 4Way Recall Summary WendyLett 4Way devices are being recalled in Canada due to a device performance issue. This is a Class II recall, meaning the product could cause temporary or medically reversible adverse effects. The affected devices were distributed across Canada.

Product
WendyLett 4Way
Reason
Device performance issue
Classification
Class II
Category
medical device recall
Country
Canada
Agency
HC-DEVICES
Recall date
2026-05-28
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/b5418491-2bc0-4113-9d3e-1d44a99b5197