Lotte Kancho Choco-Biscuits Recall: Peanut Allergen Found
Lotte International America Corp. recalls Lotte Kancho Choco-Biscuits due to peanut allergen detected in product sampling. Consumers should check UPC codes and avoid if allergic to peanuts.
Lower-risk recall
Firm was notified by customer of peanut allergen found in the product during product sampling and testing in Kancho Choco Biscuits.
Contact the company
What happened, in plain English
Lotte Kancho Choco-Biscuits have been recalled because peanut allergen was found during testing. This poses a risk for people with peanut allergies, as the product may contain traces of peanuts. Read more at govinfonow.com/recall/19642-lotte-kancho-choco-biscuits-recall-peanut-allergen-found.
Source Summary by GovInfoNow · govinfonow.com/recall/19642-lotte-kancho-choco-biscuits-recall-peanut-allergen-found · Updated October 7, 2026 · FDA enforcement record: FDA #F-0910-2018
Cite this page
“Lotte Kancho Choco-Biscuits Recall: Peanut Allergen Found.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19642-lotte-kancho-choco-biscuits-recall-peanut-allergen-found. Based on FDA recall #F-0910-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0910-2018%22&limit=1).
Why it’s dangerous
The product contains traces of peanuts that could trigger allergic reactions in sensitive individuals. This is a food safety issue for those with peanut allergies, as even small amounts can cause severe reactions.
Who’s affected
People with peanut allergies are at risk from this product. The recall affects consumers who purchased Lotte Kancho Choco-Biscuits with the specified UPC codes.
How to tell if you have this one
Check for UPC codes 8801062 144815 (42g biscuits) or 8801062 516858 (95g cup) on the packaging. The product is sold under the brand Lotte Kancho.
- Brand
Lotte Kancho- Product
Lotte Kancho Choco-Biscuit; Sold as Lotte Kancho - 42 g -1.48 oz. UPC CODE: 8801062 144815; Lotte Kancho Cup - 95 g cup- Category
Food
What to do — step by step
Check Product UPC
Look for UPC codes 8801062 144815 or 8801062 516858 on the packaging to identify affected items.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
FDA distribution: “Nationwide distribution and Canada” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA terminated this recall 9 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
What should I do if I have the recalled product?
Check the UPC codes on the packaging to confirm if you have the recalled items. If you do, avoid consumption and contact the manufacturer for further instructions.
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Where this comes from
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-0910-2018 (February 20, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0910-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 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.