RecallHawk
Class I Recall

Tiramisu Twist Cookie 3.4 oz. packaged in a gold bag with a large image of two cookies on the package. SKU 456213845082

DAISO CALIFORNIA WAREHOUSE

Summary

The FDA issued a Class I for Tiramisu Twist Cookie 3.4 oz. packaged in a gold bag with a large image of two c by DAISO CALIFORNIA WAREHOUSE. Reason: Tiramisu Twist Cookies were found to have tree nuts not declared on the label.

Details

Source

Food Recall

External ID

F-0169-2023

Action Date

2022-11-30

Status

Terminated

Category

food

Product Description

Tiramisu Twist Cookie 3.4 oz. packaged in a gold bag with a large image of two cookies on the package. SKU 4562138450820 3.4 oz. packages, 12 units per case Product of Malaysia

Lot/Code Info: All lots

Quantity Affected: 35,904 individual units

Reason for Recall

Tiramisu Twist Cookies were found to have tree nuts not declared on the label

Distribution

Product is distributed to Daiso retail locations located in Arizona, Illinois, California, Washington, Nevada, Texas, New York, and New Jersey. Product is also distributed to 2 locations in Canada.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-10-27

Company

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 28 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-0169-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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