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Health Canada Medical devices

PhiLaser Type 2.0

Issued May 31, 2023
Issue
Health Canada advised that the Philaser Type 2.0 device is considered a class III medical device and requires a licence. The Philaser Type 2.0 device is not currently licensed, so we have stopped sales and advertisement of the Philaser Type 2.0 device in Canada as of March 20, 2023. Recall start date: May 19, 2023
Hazard description
Unauthorised device
Product
Product name
PhiLaser Type 2.0
Reference
ID
RA-73735