Preime Dermafacial
Preime Dermafacial Recall Summary Preime Dermafacial products are being recalled in Canada because they are unauthorized medical devices that were sold without proper regulatory approval. This Class I recall affects all Preime Dermafacial products distributed across Canada.
- Product
- Preime Dermafacial
- Reason
- Unauthorised device
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2025-07-24
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/fe570f83-3cd3-4baf-a8ad-a8b3e6092a96