Why it was recalled
Marketed without an Approved NDA/ANDA; FDA laboratory analysis confirmed product tainted with undeclared metformin and glyburide
Product description
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
Lot numbers, UPCs & expiration codes
Batch # 001, exp. date 09/10/2026
Where it was sold
Nationwide via internet sales
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-0207-2025
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- Dec 16, 2024
- FDA report date
- Jan 29, 2025
- Quantity
- 172 180-count bottles
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- SHOPPERS- PLAZA
Original FDA data
Every field from FDA enforcement report D-0207-2025, exactly as published.
Show all FDA fields
- City
- Hawthorne
- State
- CA
- Status
- Ongoing
- Country
- United States
- Event ID
- 95994
- Address
- Fouad Panchibyaya 12816
- Code information
- Batch # 001, exp. date 09/10/2026
- Postal code
- 90250
- Report date
- Jan 29, 2025
- Product type
- Drugs
- Recall number
- D-0207-2025
- Classification
- Class I
- Recalling firm
- SHOPPERS- PLAZA
- Product quantity
- 172 180-count bottles
- Reason for recall
- Marketed without an Approved NDA/ANDA; FDA laboratory analysis confirmed product tainted with undeclared metformin and glyburide
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- 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
- Distribution pattern
- Nationwide via internet sales
- Recall initiation date
- Dec 16, 2024
- Initial firm notification
- Press Release
- Center classification date
- Jan 22, 2025