MyBlend CellSynergy
Brand(s)
Last updated
Summary
Product
MyBlend CellSynergy
Issue
Medical devices - Unauthorised device
What to do
Return the medical device to Clarins Canada Inc.
Affected products
Affected products |
Lot or serial number |
Model or catalogue number |
|---|---|---|
MyBlend CellSynergy |
Not applicable |
80095802 |
Issue
The MyBlend CellSynergy product is being recalled because they were incorrectly sold as Class I devices but should have been classified as Class II devices, and thus do not have valid medical licenses (MDL).
Recall start date: March 23, 2025
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Ophthalmology
Companies
| Myblend (Maskled) |
| 9 Rue Du Commandant Pilot, Neuilly Sur Seine, France, 92200 |
Published by
Health Canada
Audience
General public
Recall class
Type II
Identification number
RA-77358
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