Class IITerminatedVoluntary: Firm initiated
MING HONG INTERNATIONAL INC.: food recall H-0327-2025
MING HONG INTERNATIONAL INC. of City Of Industry, CA recalled Sushi Wasabi; 5 grams (Ready to eat) Ingredients: Horseradish, Corn Oil, Salt, Water, Citric Acid, Tumeric, FD&C… Reason: Individual consumer size Wasabi mini pack label does not declare allergen ingredient Yellow 5. The FDA listed it as Class II in its Enforcement Report dated Jul 30, 2025; distribution: California, Colorado, Florida, Guam, Hawaii, Illinois, Indiana, Kansas, Michigan, Minnesota, Missouri, North Carolina, New Mexico, Nevada, Ohio, Oklahoma, Oregon, Pennsylvania, Texas, Utah, Washington.
Record status as published: Terminated (terminated Jun 18, 2026). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- Sushi Wasabi; 5 grams (Ready to eat) Ingredients: Horseradish, Corn Oil, Salt, Water, Citric Acid, Tumeric, FD&C Blue#1 Distributed by: Tokyo Nori U.S.A, City of Industry, CA 91746
- Product quantity
- 1848 cases (2000 packs/case)
- Reason for recall
- Individual consumer size Wasabi mini pack label does not declare allergen ingredient Yellow 5.
- Codes, lots and dates on the package
- Lot number is best by date: 02/09/2024 which is formatted DD/MM/YYYY
- Distribution pattern
- Product was distributed to wholesale distributors, retail customers, and restaurants in the following States: Lot April 20, 2024- CA, WA, OR, TX, MN, NV, IN, IL, MI, PA, HI, NM, MO CO, FL, KS, UT, NC, BARBADOS, CANADA, GUAM Lot September 2, 2024- CA, FL, HI, IL, MI, MN, NC, NV, OH, OK, OR, TX, UT, WA, GUAM, CANADA, COSTA RICA,
- Recalling firm
- MING HONG INTERNATIONAL INC., City Of Industry, CA
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Jul 16, 2025 |
| Classified by the FDA | Jul 23, 2025 |
| Published in the Enforcement Report | Jul 30, 2025 |
| Terminated | Jun 18, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0327-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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