YO!MAN CUCUMBER (FRESH HUNAN FLAVOR); Ingredients: Cucumber, chili pepper, edible vegetable oil, salt, water, sugar, bre
Summary
The FDA issued a Class III for YO!MAN CUCUMBER (FRESH HUNAN FLAVOR); Ingredients: Cucumber, chili pepper, edibl by TENGEN USA TRADING CORP. Reason: Product contains undeclared cyclamates..
Details
Source
Food Recall
External ID
H-0525-2026
Action Date
2026-03-04
Status
Terminated
Category
food
Product Description
YO!MAN CUCUMBER (FRESH HUNAN FLAVOR); Ingredients: Cucumber, chili pepper, edible vegetable oil, salt, water, sugar, brewing vinegar, food additives (monosodium glutamate, sodium dehydroacetate, potassium sorbate, streptoccoccus lactis, sodium D-isoacsorbate, disodium ethylenediaminetetraacetatic acid, sodium metabisulphite, citric acid, lactic acid, glacial acetic acid, xanthan gum), food flavors and fragrances; NET WT. 4.42oz.(125g); SHELF LIFE: 10 MONTHS; PRODUCT OF CHINA; Distributed by: Tengen USA Trading Corp 262 48th Street,Brooklyn,NY 11220; UPC: 4 895235 529602
Lot/Code Info: 2024 -08-01 (production date)
Quantity Affected: 26 cases
Reason for Recall
Product contains undeclared cyclamates.
Distribution
NY, PA, FL, LA, TX
Type: Voluntary: Firm initiated
Recall Initiated: 2025-09-23
Company
Brooklyn, NY
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 27 food recalls issued in the same week, part of 204 food-related FDA actions this month.
TENGEN USA TRADING CORP has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (TENGEN USA TRADING CORP) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does TENGEN USA TRADING CORP have FDA actions?
TENGEN USA TRADING CORP has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0525-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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