FEG Eyelash Enhancer: Unauthorized Product with ingredient on prescription drug list.
Last updated
Summary
Product
FEG Eyelash Enhancer
Issue
Health products - Unauthorized product
What to do
Consult your healthcare provider prior to discontinuing use of the affected product, or for any health concerns.
Distribution
Alberta
British Columbia
New Brunswick
Nova Scotia
Ontario
Prince Edward Island
Quebec
Saskatchewan
Affected products
Brand |
Product Name |
Market Authorization |
Dosage Form |
Strength |
Lot |
|---|---|---|---|---|---|
FEG Eyelash Enhancer |
FEG Eyelash Enhancer |
Not Licensed |
Solution |
FEG Eyelash Enhancer |
All lots |
Issue
| Product sold without market authorization (DIN) in Canada. Product contains undeclared ingredient, bimatoprost, that is listed on the prescription drug list |
What you should do
- Verify if your product is affected.
- Contact the recalling firm if you have any questions about the recall.
- Report any health product related side effects to Health Canada.
- Report any other health product safety complaints to Health Canada.
- Report any other health product safety complaints to Health Canada.
Additional information
Background
Depth of recall: Wholesalers, Retailers
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Drugs
Companies
Toronto Lash Supplies
608 Wellington St. W,
Toronto, Ontario
M5V2X5
Published by
Health Canada
Audience
General public
Healthcare
Industry
Distribution
Alberta
British Columbia
New Brunswick
Nova Scotia
Ontario
Prince Edward Island
Quebec
Saskatchewan
Recall class
Type II
Identification number
RA-74152
Get notified
Receive notifications for new and updated recalls and alerts by category.