Recall MonitorHealth Products
Preime Dermafacial
· Published by Health Canada · Official notice
Details
Alert type: Health product recall
Category: Health products - Medical devices - General and plastic surgery
Product: Preime Dermafacial
Issue: Medical devices - Unauthorised device
What to do: Cease use of device until Medical Device License (MDL) is issued.
Audience: General public
Recall class: Type II
Products
| Affected products | Lot or serial number | Model or catalogue number |
|---|---|---|
| Preime Dermafacial | Not applicable. | 4001 |
Issue
The Preime Dermafacial is being recalled as they were incorrectly sold as electronic devices but should have been classified as Class II/Class III devices, and thus do not have a valid Medical Device License (MDL). There is no defect to the products. Recall start date: June 30, 2025