Meito Milk Cocoa 12gX5P (1stick bonus pack) UPC: 4902757444709 Made in Japan
Summary
The FDA issued a Class II for Meito Milk Cocoa 12gX5P (1stick bonus pack) UPC: 4902757444709 Made in Japan by DAISO CALIFORNIA WAREHOUSE. Reason: The allergen of coconut was not declared on the label..
Details
Source
Food Recall
External ID
F-0637-2023
Action Date
2023-03-29
Status
Terminated
Category
food
Product Description
Meito Milk Cocoa 12gX5P (1stick bonus pack) UPC: 4902757444709 Made in Japan
Lot/Code Info: No code information on product
Quantity Affected: 249 units
Reason for Recall
The allergen of coconut was not declared on the label.
Distribution
California, Washington, Nevada, Texas, New York, New Jersey, Canada.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-02-10
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 503 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-0637-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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