Summary
The FDA issued a Class II for Tohato 5packs of Caramel Corn 23g units UPC:4901940111145 by DAISO CALIFORNIA WAREHOUSE. Reason: Almond listed on the ingredient label but is not in Contains statement..
Details
Source
Food Recall
External ID
F-0375-2023
Action Date
2023-03-01
Status
Terminated
Category
food
Product Description
Tohato 5packs of Caramel Corn 23g units UPC:4901940111145
Lot/Code Info: No code on package
Quantity Affected: 317,751 total units
Reason for Recall
Almond listed on the ingredient label but is not in Contains statement.
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 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 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 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 (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-0375-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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