Philaser Type 2.0
PhiLaser Type 2.0 Recall Summary The PhiLaser Type 2.0 is being recalled across Canada because it is an unauthorized medical device that was sold without proper approval. This is a Class I recall, the most serious type. The device was distributed throughout Canada.
- Product
- PhiLaser Type 2.0
- Reason
- Unauthorised device
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2023-05-31
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/2302f51c-88b5-48b0-8d50-b828cb5731e1