Korean Sushi, net wt. 12 oz. UPC 0 72148 48043 3. The label is read in parts: "***KOREAN SUSHI ***Ingredients: Rice,
Summary
The FDA issued a Class II for Korean Sushi, net wt. 12 oz. UPC 0 72148 48043 3. The label is read in parts: by Han Yang Corp.. Reason: Undeclared Yellow #5..
Details
Source
Food Recall
External ID
F-0614-2022
Action Date
2022-02-02
Status
Terminated
Category
food
Product Description
Korean Sushi, net wt. 12 oz. UPC 0 72148 48043 3. The label is read in parts: "***KOREAN SUSHI ***Ingredients: Rice, Seaweed, Water, Salt, Eggs, Sesame Oil, Spinach, Carrot, Yellow Radish, and Sesame Seed. *** Han Yang Oriental Food Mfg. 3819 94th St. SW, Tacoma, WA 98499 (253) 588-7303***".
Lot/Code Info: EXPIRES JAN 14 8:00 AM
Quantity Affected: 61 packages
Reason for Recall
Undeclared Yellow #5.
Distribution
Distributed in WA only.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-01-13
Company
Lakewood, WA
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 117 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 (Han Yang Corp.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Han Yang Corp. have FDA actions?
This is the only FDA action we have on record for Han Yang Corp. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0614-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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