RecallHawk
Class III Recall

Fujiya Country Ma'am Vanilla & Cocoa 19 sheets UPC: 4902555272641

DAISO CALIFORNIA WAREHOUSE

Summary

The FDA issued a Class III for Fujiya Country Ma'am Vanilla & Cocoa 19 sheets UPC: 4902555272641 by DAISO CALIFORNIA WAREHOUSE. Reason: Sheanut is not listed in the ingredients list or on the contains statement.

Details

Source

Food Recall

External ID

F-0880-2023

Action Date

2023-05-17

Status

Terminated

Category

food

Product Description

Fujiya Country Ma'am Vanilla & Cocoa 19 sheets UPC: 4902555272641

Lot/Code Info: No code on package

Quantity Affected: 46 units

Reason for Recall

Sheanut is not listed in the ingredients list or on the 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

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-0880-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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