RecallHawk
Class II Recall

Sushi Wasabi; 5 grams (Ready to eat) Ingredients: Horseradish, Corn Oil, Salt, Water, Citric Acid, Tumeric, FD&C Blue#1

MING HONG INTERNATIONAL INC.

Summary

The FDA issued a Class II for Sushi Wasabi; 5 grams (Ready to eat) Ingredients: Horseradish, Corn Oil, Salt, W by MING HONG INTERNATIONAL INC.. Reason: Individual consumer size Wasabi mini pack label does not declare allergen ingredient Yellow 5..

Details

Source

Food Recall

External ID

H-0327-2025

Action Date

2025-07-30

Status

Terminated

Category

food

Product Description

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

Lot/Code Info: Lot number is best by date: 02/09/2024 which is formatted DD/MM/YYYY

Quantity Affected: 1848 cases (2000 packs/case)

Reason for Recall

Individual consumer size Wasabi mini pack label does not declare allergen ingredient Yellow 5.

Distribution

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,

Type: Voluntary: Firm initiated

Recall Initiated: 2025-07-16

Company

MING HONG INTERNATIONAL INC.

City Of Industry, CA

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 71 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

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 (MING HONG INTERNATIONAL INC.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does MING HONG INTERNATIONAL INC. have FDA actions?

This is the only FDA action we have on record for MING HONG INTERNATIONAL INC. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0327-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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