DAISO CALIFORNIA WAREHOUSE Recall: The allergen of wheat was not declared on the label. (firm stated that soy was not declared as well, but upon review, soy was listed on the ingredient label)

🇺🇸 United States

1. February 10, 2023 - Recall initiated
2. March 29, 2023 - Reported by source
3. May 3, 2024 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0632-2023

Event ID

91699

Status

Terminated

Classification

Class I

Company

DAISO CALIFORNIA WAREHOUSE

Product description

IWATSUKASEIKA Soybean flavor 72g -21pieces UPC: 4901037131919 Made in Japan

Quantity

4,498 units

Reason

The allergen of wheat was not declared on the label. (firm stated that soy was not declared as well, but upon review, soy was listed on the ingredient label)

Recall initiation date

February 10, 2023

Report date

March 29, 2023

Classification date

Not published in this source record

Termination date

May 3, 2024

Distribution pattern

California, Washington, Nevada, Texas, New York, New Jersey, Canada.

UPC, lot, and code information

UPC 4901037131919; No code information on product

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 91699 with 10 other product entries in Public Health Trace.

Responsible company: DAISO CALIFORNIA WAREHOUSE

Other recalls from DAISO CALIFORNIA WAREHOUSE

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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