Yo!man Cucumber
Reason Product contains undeclared cyclamates.
Yo!man Lettuce recall
Recalled by Tengen USA Trading CORP · Brooklyn, NY, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Product contains undeclared cyclamates.
See the recall's own reason text for the specifics. All other reasons recalls.
What was recalled
YO!MAN LETTUCE (SPICY FLAVOR); Ingredients: Lettuce, chili pepper, edible vegetable oil, salt, water, sugar, food additives (monosodium glutamate, potassium sorbate, streptoccoccus lactis, sodium dehydroacetate, sodium D-isoacsorbate, disodium ethylenediaminetetraacetatic acid, sodium metabisulphite, citric acid, lactic acid, glacial acetic acid, sucralose, xanthan gum, disodium 5'flavoring ribonucleotide), food flavors and fragrances; NET WT. 4.42oz.(125g); SHELF LIFE: 9 MONTHS; PRODUCT OF CHINA; Distributed by: Tengen USA Trading Corp 262 48th Street,Brooklyn,NY 11220; UPC: 4 895235 529626
Quantity: 26 cases
Food: Leafy greens & salads
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
2024-08-01 (production date)
Where it was sold
Florida Louisiana New York Pennsylvania Texas
FDA's distribution note: NY, PA, FL, LA, TX
Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Tengen USA Trading CORP
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Sep 23, 2025
- In FDA report of
- Mar 4, 2026
- Terminated
- Mar 13, 2026
- FDA recall number
- H-0526-2026 · event 98357
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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