FDA recall record

MEI YU CHENG DA TRADING DADI NONGFU DRIED SALT CHILLI VEGETABLE recall — FDA H-0657-2026

Products contain banned sweetener: cyclamates.

Class IIIclassification
H-0657-2026official record ID
Apr 15, 2026report date

Recall record at a glance

Official recordH-0657-2026
CategoryFood Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmMEI YU CHENG DA TRADING INC
Report dateApr 15, 2026
Recall initiation dateNov 13, 2025
Quantity29 cases (total)
LocationWestbury, NY, United States

Official product description

DADI NONGFU DRIED SALT CHILLI VEGETABLE(S); Ingredients: Radish, chili, roasted sesame, prickly ash, edible salt, soybean oil, edible vinegar, white granulated sugar, spices, food additives (sodium glutamate, citric acid, sodium benzoate, potassium sorbate, sodium saccharin, acesulfame, sucralose, disodium EDTA, turmeric).; Allergen: This product contains sesame and soy products; Net Wt. 14.1 oz(400g)

Why the product was recalled

Products contain banned sweetener: cyclamates.

Distribution information

NY, PA, FL

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.