myLEDmask was registered as a Class I device and Health Canada considers it should be Class II. This Type II recall is a precautionary measure, as the device was not submitted under Class II and in the absence of evidence to the contrary, the device may pose potential health risks. No adverse events have been reported in Canada to date.

If you purchased your LED Mask in Canada, please contact our customer service.

This recall does not apply to other countries.