Endoflip System

Endoflip System Recall Summary The Endoflip System, a medical device distributed across Canada, is being recalled due to a device performance issue. This is a Class I recall, indicating a serious problem with how the device functions. The recall affects all Canadian users of this equipment.

Product
Endoflip System
Reason
Device performance issue
Classification
Class I
Category
medical device recall
Country
Canada
Agency
HC-DEVICES
Recall date
2026-05-14
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/0e256797-d85c-4f93-8bb8-ff13fc3ae6e1