CLASS I Food recall · Reported 1 Mar 2023 · FDA Enforcement Report

Kanro Pure gummy Petit trigonal pyramid grape recalled

Daiso California Warehouse is recalling Kanro Pure gummy Petit trigonal pyramid grape, distributed in California, New Jersey, Nevada, New York, Texas, Washington. The recall was initiated on 3 Feb 2023 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesNo code
Quantity recalled113,205 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-0381-2023
FDA event ID
91644
Recalling firm
Daiso California Warehouse, La Mirada, CA
Brand
Kanro
Classification
Class I
Status
Terminated
Recall initiated
3 Feb 2023
FDA classified
22 Feb 2023
Reported
1 Mar 2023
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Soy
Product category
Candy

Timeline

3 Feb 2023Recall initiated by company
22 Feb 2023Classified by FDA+19 days
1 Mar 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

Products were found to contain allergens that are not listed on the label, undeclared soy.

Product as listed by the FDA

KANRO Pure gummy Petit trigonal pyramid grape 17g 3 pieces UPC: 4901351055489

Where it was distributed

Daiso stores in California, Washington, Nevada, Texas, New York, and New Jersey. also, 3 stores in British Columbia, Canada

CaliforniaNew JerseyNevadaNew YorkTexasWashington

Questions about this recall

Why was it recalled?

Products were found to contain allergens that are not listed on the label, undeclared soy.

Which lots are affected?

No code

Where was it sold?

Daiso stores in California, Washington, Nevada, Texas, New York, and New Jersey. also, 3 stores in 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 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

4 other products · FDA event 91644

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