CLASS I Food recall · Reported 17 May 2023 · FDA Enforcement Report

Kimura burdock salt recalled by Daiso California Warehouse

Daiso California Warehouse is recalling Kimura burdock salt, distributed in California, New Jersey, Nevada, New York, Texas, Washington. The recall was initiated on 3 Mar 2023 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesNo code on package
Quantity recalled561 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0876-2023
FDA event ID
91843
Recalling firm
Daiso California Warehouse, La Mirada, CA
Brand
Kimura
Classification
Class I
Status
Terminated
Recall initiated
3 Mar 2023
FDA classified
10 May 2023
Reported
17 May 2023
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Product category
Other

Timeline

3 Mar 2023Recall initiated by company
10 May 2023Classified by FDA+68 days
17 May 2023Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Fish (Sardines, Bonito, Tuna) not listed either in ingredients list or in the contains statement

Product as listed by the FDA

Kimura burdock salt 40g UPC: 4972304293524

Where it was distributed

Products were distributed to customer retail locations in California, Texas, Nevada, New York, New Jersey, Washington, and British Columbia Canada.

CaliforniaNew JerseyNevadaNew YorkTexasWashington

Questions about this recall

Is Kimura burdock salt recalled?

Yes. Daiso California Warehouse recalled Kimura burdock salt on 3 Mar 2023. The recall is Class I and its status is Terminated. Recall number F-0876-2023.

Why was it recalled?

Fish (Sardines, Bonito, Tuna) not listed either in ingredients list or in the contains statement

Which lots are affected?

No code on package

Where was it sold?

Products were distributed to customer retail locations in California, Texas, Nevada, New York, New Jersey, Washington, and British Columbia Canada.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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