Chirashi Sauce packaged in 1/2 gallon plastic jug. Label read in parts: "Korean hot bean paste, Reg. Vinegar, Sugar, Sa
Summary
The FDA issued a Class I for Chirashi Sauce packaged in 1/2 gallon plastic jug. Label read in parts: "Korean by Joonsung Trading Inc. Reason: Undeclared soy and wheat. Label declares Hot Bean Paste but does not declare Soy and Wheat..
Details
Source
Food Recall
External ID
F-1077-2022
Action Date
2022-06-01
Status
Terminated
Category
food
Product Description
Chirashi Sauce packaged in 1/2 gallon plastic jug. Label read in parts: "Korean hot bean paste, Reg. Vinegar, Sugar, Sake, Garlic powder, 7up".
Lot/Code Info: The product with a date prior to APR 14 2022 is recalled.
Quantity Affected: 1 container (1/2 gallon)
Reason for Recall
Undeclared soy and wheat. Label declares Hot Bean Paste but does not declare Soy and Wheat.
Distribution
Distributed in Oregon and Washington
Type: Voluntary: Firm initiated
Recall Initiated: 2022-04-14
Company
Portland, OR
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 27 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Joonsung Trading Inc has 5 FDA actions in our database, including 5 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (Joonsung Trading Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Joonsung Trading Inc have FDA actions?
Joonsung Trading Inc has 5 FDA actions in our database, including 5 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1077-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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