Summary
The FDA issued a Class I for Caramel Corn Boys Festival 80g units UPC:4901940039432 by DAISO CALIFORNIA WAREHOUSE. Reason: Product contains almonds and peanuts that were not listed on the ingredient label..
Details
Source
Food Recall
External ID
F-0366-2023
Action Date
2023-03-01
Status
Terminated
Category
food
Product Description
Caramel Corn Boys Festival 80g units UPC:4901940039432
Lot/Code Info: No code on package
Quantity Affected: 317,751 total units
Reason for Recall
Product contains almonds and peanuts that were not listed on the ingredient label.
Distribution
Product is distributed to 88 Daiso retail stores located in the states of CA, WA, Nevada, TX, NY, and NJ, and 2 locations in Vancouver, Canada
Type: Voluntary: Firm initiated
Recall Initiated: 2023-01-10
Company
La Mirada, CA
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 37 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 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 (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-0366-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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