FDA recall record

DAISO CALIFORNIA WAREHOUSE Ribbon raw thigh candy 65g UPC: 4903316410630 recall — FDA F-0869-2023

"Fish" listed in both ingredients list and contains statement; no species identified

Class IIIclassification
F-0869-2023official record ID
May 17, 2023report date

Recall record at a glance

Official recordF-0869-2023
CategoryFood Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmDAISO CALIFORNIA WAREHOUSE
Report dateMay 17, 2023
Recall initiation dateMar 3, 2023
Quantity12,589 units
LocationLa Mirada, CA, United States

Official product description

Ribbon raw thigh candy 65g UPC: 4903316410630

Why the product was recalled

"Fish" listed in both ingredients list and contains statement; no species identified

Distribution information

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

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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.

Related recall records

Other records from the same recalling company are shown first when available.