Philips Allura Xper Fd Series
Philips Allura Xper FD Series Recall Summary Philips is recalling the Allura Xper FD series of medical imaging devices across Canada due to a device performance issue. This recall is classified as Class II, meaning the device could cause serious adverse health consequences or death. The affected devices are distributed throughout Canada.
- Product
- Philips Allura Xper FD series
- Reason
- Device performance issue
- Classification
- Class II
- Category
- medical device recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2026-07-16
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/85c58269-6bf6-42fe-8490-987ef9fb88b1