FDA Drugs recall ·
FOUZEE SugarLin HERBAL FORMULA capsules, 180 capsules per bottle… recall
This is an FDA Class I recall — the most serious type.
- Recall number
- D-0207-2025
- Date
- (initiated December 16, 2024)
- Company / brand
- Shoppers- Plaza
Fouad Panchibyaya 12816, Hawthorne, CA, United States - Category
- Drugs › Class I
- Classification
- Class I
- Status
- Ongoing
- Units affected
- 172 180-count bottles
- Hazard tags
- Undeclared allergen
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
FOUZEE SugarLin HERBAL FORMULA capsules, 180 capsules per bottle, Sold and Distributed by Shoppers-Plaza, Hawthorne, CA 90250. Product of India. UPC 8 26656 69047 7
Why was it recalled?
Marketed without an Approved NDA/ANDA; FDA laboratory analysis confirmed product tainted with undeclared metformin and glyburide
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Batch # 001, exp. date 09/10/2026
Distribution
Nationwide via internet sales
What does Class I mean?
Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Source: FDA (drugs), recall D-0207-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.