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Preime dermafacial
Official notice
24 Jul 2025
Last checked
24 Jul 2025
An official Health Canada notice concerns Preime dermafacial. 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 Published 2025-07-24.
What to do now
Cease use of device until Medical Device License (MDL) is issued.
Recall number
77757
Official notice
2025-07-24
The hazard
The hazard
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
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
Recall Numbers
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Turn on recall alertsAffected products
Affected products
Product 1
Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Brand: Ema Aesthetics, Preime Dermafacial.
Source & status
Source & status
Source
Tier
Category
Classification
App estimate
Recall details
Recall details
Recall number
Classification
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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