The FDA has identified this as a Class I recall, t..

3 år

The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.

Why TF isn't the school boards that sent these things home with our children informing families of this?! I'm emailing both the schools and our school board.

Canadian link

https://recalls-rappels.canada.....ca/en/alert-recall/

FDA link
https://www.fda.gov/medical-de....vices/medical-device