RecallHawk
Class I Recall

Takuma food herb salt peanut 80g UPC: 4962679652767

DAISO CALIFORNIA WAREHOUSE

Summary

The FDA issued a Class I for Takuma food herb salt peanut 80g UPC: 4962679652767 by DAISO CALIFORNIA WAREHOUSE. Reason: no fish (Bonito, Sardines, Tuna) listed on ingredients or contains statement.

Details

Source

Food Recall

External ID

F-0871-2023

Action Date

2023-05-17

Status

Terminated

Category

food

Product Description

Takuma food herb salt peanut 80g UPC: 4962679652767

Lot/Code Info: No code on package

Quantity Affected: 779 units

Reason for Recall

no fish (Bonito, Sardines, Tuna) listed on ingredients or 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 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 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 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-0871-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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