Summary
The FDA issued a Class III for Daisho Kimchi hotpot soup 750g UPC: 4904621042653 by DAISO CALIFORNIA WAREHOUSE. Reason: Label warns for fish but does not specify anchovy or sardine; Canada lists clams in ingredients but not in contains statement..
Details
Source
Food Recall
External ID
F-0868-2023
Action Date
2023-05-17
Status
Terminated
Category
food
Product Description
Daisho Kimchi hotpot soup 750g UPC: 4904621042653
Lot/Code Info: No code on package
Quantity Affected: 4,078 units
Reason for Recall
Label warns for fish but does not specify anchovy or sardine; Canada lists clams in ingredients but not in contains statement.
Distribution
Products were distributed to customer retail locations in California, Texas, Nevada, New York, New Jersey, Washington, and British Columbia Canada.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-03-03
Company
La Mirada, CA
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 111 food recalls issued in the same week, part of 204 food-related FDA actions this month.
DAISO CALIFORNIA WAREHOUSE has 58 FDA actions in our database, including 58 recalls.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
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 (DAISO CALIFORNIA WAREHOUSE) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does DAISO CALIFORNIA WAREHOUSE have FDA actions?
DAISO CALIFORNIA WAREHOUSE has 58 FDA actions in our database, including 58 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0868-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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