Feather Dream Mint CBD Rapid Spray; No Market Authorization
Brand(s)
Last updated
Summary
Product
Feather Dream Mint CBD Rapid Spray
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.
Affected products
Brand |
Product Name |
Market Authorization |
Dosage Form |
Strength |
Lot number |
|---|---|---|---|---|---|
Feather |
Dream Mint CBD Rapid Spray |
No market authorization |
Spray |
CBD 400 mg |
S80FTHDM22043 |
Issue
Product sold without market authorization (DIN) in Canada.
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.
Additional information
Background
Depth of recall: Retailers
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Drugs
Companies
Motif Labs Ltd.
516 John Street North
Aylmer ON N6H 2B8 Canada
Published by
Health Canada
Audience
General public
Healthcare
Industry
Recall class
Type II
Identification number
RA-73723
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