Philips Allura Xper Systems

Philips Allura Xper Systems Recall Philips Allura Xper Systems, which are medical imaging devices used in hospitals and clinics across Canada, are being recalled due to a device performance issue. This is a Class II recall, meaning the issue could potentially cause adverse health effects but is not immediately life-threatening. The recall affects all Philips Allura Xper Systems distributed throughout Canada.

Product
Philips Allura Xper Systems
Reason
Device performance issue
Classification
Class II
Category
medical device recall
Country
Canada
Agency
HC-DEVICES
Recall date
2026-06-04
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/5bb065eb-66a9-4a22-b5fe-f95ade76fdb0