CLASS I ONGOING Drug recall · Reported 29 Jan 2025 · FDA Enforcement Report
Fouzee SugarLin Herbal Formula capsules per, Sold recalled
Shoppers- Plaza is recalling Fouzee SugarLin Herbal Formula capsules per, Sold, distributed nationwide in the US. The recall was initiated on 16 Dec 2024 and the FDA has classified it as Class I.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0207-2025
- FDA event ID
- 95994
- Recalling firm
- Shoppers- Plaza, Hawthorne, CA
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 16 Dec 2024
- FDA classified
- 22 Jan 2025
- Reported
- 29 Jan 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Labeling Errors
Timeline
| 16 Dec 2024 | Recall initiated by company | |
| 22 Jan 2025 | Classified by FDA | +37 days |
| 29 Jan 2025 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Marketed without an Approved NDA/ANDA; FDA laboratory analysis confirmed product tainted with undeclared metformin and glyburide
Product as listed by the FDA
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
Where it was distributed
Nationwide via internet sales
Stores named: Online Retailers
Questions about this recall
Is Fouzee SugarLin Herbal Formula capsules per, Sold recalled?
Yes. Shoppers- Plaza recalled Fouzee SugarLin Herbal Formula capsules per, Sold on 16 Dec 2024. The recall is Class I and its status is Ongoing. Recall number D-0207-2025.
Why was it recalled?
Marketed without an Approved NDA/ANDA; FDA laboratory analysis confirmed product tainted with undeclared metformin and glyburide
Which lots are affected?
Batch # 001, exp. date 09/10/2026
Where was it sold?
Nationwide via internet sales
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.