← FDA ENFORCEMENT
D-0207-2025Class I

SHOPPERS- PLAZA

Recalling firm
SHOPPERS- PLAZA
Product type
Drug
Status
Ongoing
Report date
2025-01-29
Distribution
Nationwide via internet sales
Firm state
CA
Product quantity
172 180-count bottles
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Documentation & Change Control
Reason for recall

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

Code / lot info

Batch # 001, exp. date 09/10/2026

Other recalls SPEQ maps to Documentation & Change Control
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See all Documentation & Change Control recalls →

Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.