MEITO An extra Stick Powdered Lemon Tea 5packs UPC: 4902757442804 Made in Japan
Summary
The FDA issued a Class I for MEITO An extra Stick Powdered Lemon Tea 5packs UPC: 4902757442804 Made in Japan by DAISO CALIFORNIA WAREHOUSE. Reason: The allergen of milk was not declared on the label..
Details
Source
Food Recall
External ID
F-0633-2023
Action Date
2023-03-29
Status
Terminated
Category
food
Product Description
MEITO An extra Stick Powdered Lemon Tea 5packs UPC: 4902757442804 Made in Japan
Lot/Code Info: No code information on product
Quantity Affected: 4,411 units
Reason for Recall
The allergen of milk 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 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 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 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-0633-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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