NazalActin Liquid: No market authorization, incorrect NPN, deficiencies in Good Manufacturing Practices
Brand(s)
Last updated
Summary
Product
NazalActin Liquid
Issue
Health products - Product quality
What to do
Consult your health care professional if you have any health concerns.
Affected products
| Brand | Product Name | Market Authorization | Dosage Form | Strength | Lot number |
|---|---|---|---|---|---|
| Sunforce Health & Organics | NazalActin Liquid | No market authorization | Liquid | Silver 50 mcg | 22S2302 |
Issue
Product sold without market authorization (NPN) in Canada. Affected lot is labelled with the incorrect NPN found on the label. Quality concerns of affected lots due to deficiencies in Good Manufacturing Practices (GMP).
What you should do
- Verify if your product is affected.
- Consult your healthcare provider prior to discontinuing use of the affected product(s), or for any health concerns.
- 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.
Related recalls and alerts
Additional information
Background
Depth of recall: Retailers
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Natural health products
Companies
Recalling Firm:
Ecotrend Ecologics Ltd.
125 W 3rd Ave,
Vancouver, BC V5Y 1E6 Canada
Marketing Authorization Holder:
SunForce Health & Organics Inc.
5323 - 273 A Street,
Langley Twp, BC V4W 3Z4 Canada
Published by
Health Canada
Audience
General public
Healthcare
Industry
Recall class
Type III
Identification number
RA-78036
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