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