Suji's Korean Cuisine recalls Taiyaki Variety Pack (21.6 oz) due to hazelnuts listed in ingredients but not in the Contains statement, posing an allergen risk for sensitive individuals.
“Suji's Korean Cuisine Taiyaki Variety Pack Recall: Missing Hazelnut Allergen Label.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/13328-suji-s-korean-cuisine-taiyaki-variety-pack-recall-missing-hazelnut. Based on FDA recall #F-0898-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0898-2022%22&limit=1).
The FDA announced on Feb. 17, 2022, that FDMR, Inc. d/b/a Suji's Korean Cuisine recalled Taiyaki Variety Pack due to undeclared hazelnuts. The agency said the product was distributed nationwide.
How to tell if you have it
Brand: Suji's Korean Cuisine
Product: 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
The hazard
Hazelnuts were declared in the ingredient statement but not in the Contains statement, according to the FDA. The recall is classified as Class II.
Context
GovInfoNow's records show other recent recalls of similar products include Albertsons Strawberry Shortcake Triangle Recall (2026-05-06), Albertsons Chocolate Covered Strawberries Recall (2026-05-06) and Albertsons Pop Dots Coco & Hazelnut 6ct Recall (2026-05-06).
How to tell if you have this one
Check for the Taiyaki Variety Pack (21.6 oz) with three flavors: Chocolate Cream, Vanilla Custard, and Red Bean & Cinnamon. The product was manufactured in Republic of Korea and sold under the brand Suji's Korean Cuisine.
Brand
Suji's Korean Cuisine
Product
Taiyaki Variety Pack; 21.6 oz. (600g) 30 fish waffles in a units, 27 master cased to a pallet, 40 pallets to container
Category
Food
Based on the official FDA remedy
What to do — step by step
Check for Allergen Label
Verify the 'Contains' statement on the product label to ensure hazelnuts are listed. If not, stop using the product.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 46 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “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.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, District of Columbia, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, Wisconsin.
Recall timeline
FDA terminated this recall 5 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #F-0898-2022 (February 17, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0898-2022 to see it in context.
Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.