Llura Xper Products (2016-04-05)
Allura Xper Products Recall Summary Allura Xper medical devices were recalled across Canada in April 2016 due to safety concerns classified as Class I, the most serious type of recall. The recall affected all Allura Xper products distributed in Canada. This is a medical device recall, meaning the products are used for medical purposes.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2016-04-22
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/84e0071a-1b3a-4a95-8b17-02848bf2579e