FDA recall record

DAISO CALIFORNIA WAREHOUSE TOHATO Bitter Caramel Corn 77g units UPC:4901940111121 recall — FDA F-0369-2023

Product contains almonds that are not listed on the ingredient label.

Class Iclassification
F-0369-2023official record ID
Mar 1, 2023report date

Recall record at a glance

Official recordF-0369-2023
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmDAISO CALIFORNIA WAREHOUSE
Report dateMar 1, 2023
Recall initiation dateJan 10, 2023
Quantity317,751 total units
LocationLa Mirada, CA, United States

Official product description

TOHATO Bitter Caramel Corn 77g units UPC:4901940111121

Why the product was recalled

Product contains almonds that are not listed on the ingredient label.

Distribution information

Product is distributed to 88 Daiso retail stores located in the states of CA, WA, Nevada, TX, NY, and NJ, and 2 locations in Vancouver, Canada

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Press Release.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

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