FDA recall record

FDMR, INC DBA SUJI'S KOREAN CUISINE Taiyaki Pack recall — FDA F-0898-2022

Hazelnuts were declared in ingredient statement but not in Contains statement.

Class IIclassification
F-0898-2022official record ID
Mar 23, 2022report date

Recall record at a glance

Official recordF-0898-2022
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmFDMR, INC DBA SUJI'S KOREAN CUISINE
Report dateMar 23, 2022
Recall initiation dateFeb 17, 2022
Quantity63,451sold
LocationChicago, IL, United States

Official product description

Taiyaki Variety Pack; 21.6 oz. (600g) 30 fish waffles in a units, 27 master cased to a pallet, 40 pallets to container. Item Number 1598329, UPC: 8 50013 07258 3 Three flavors: Chocolate Cream, Vanilla Custard and Red Bean & Cinnamon. Manufactured for Suji's Korean Cuisine, Seattle, WA Country of Origin: Republic of Korea.

Why the product was recalled

Hazelnuts were declared in ingredient statement but not in Contains statement.

Distribution information

Nationwide to wholesale customer locations in AK, AL,AR,AZ,CA,CO,CT,DC, DE,FL, GA, HI,IA, ID, IL, IN, KS, KY,LA,MA,MD, MI, MN, MO, MS, MT, NA, NC, ND,NE, NH, NJ, NM, NV, NY, OH,OK,OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

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.