Class ITerminated in FDA datasetFeb 20, 2018

Lotte Kancho Choco-Biscuit; Sold as Lotte Kancho - 42 g -1.48 oz.

Recalling firm: Lotte International America Corp.

Why it was recalled

Firm was notified by customer of peanut allergen found in the product during product sampling and testing in Kancho Choco Biscuits.

Check the codes ↓

The exact product

Lotte Kancho Choco-Biscuit; Sold as Lotte Kancho - 42 g -1.48 oz. UPC CODE: 8801062 144815; Lotte Kancho Cup - 95 g cup - UPC CODE: 8801062 516858; Lotte Kancho Multi - 168 g - UPC CODE: 8801062 144815. Master carton UPC: 1 8801062 133090 Ingredients: Wheat Flour, Sugar, Blended oil (hydrogenated palm oil, Palm oil, Glycerin esters of fatty acid, Tocopherol), Cocoa mass, Palm oil, Cocoa preparation (Whole milk powder, Cocoa mass), Lactose Acidity regulator (Ammonium bicarbonate, Sodium bicarbonate), Dextrin, Almond powder, Processed whole milk powder (Whey powder, Butter fat, Lactose, Milk cream, Sodium caseinate), Salt, D-altritol, Artificial flavors, Emulsifier (Soy lecithin), Yeast preparation (Glucose syrup, Sugar, Water), Protease preparation (Protease, Glycerol) Allergen Information: Contain wheat, Soy, Milk, Almond, May contain Egg Distributed by Lotte Int'l America Corp., Los Angeles, CA 90021

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

Match the product, size and code together. A similar name alone does not identify your batch.

Original FDA code information

All codes Product ID #: 10142080

Recall details

Recall number
F-0910-2018
Event ID
79312
FDA status
Terminated
Initiated
Feb 20, 2018
Reported
Mar 14, 2018
Classified
Mar 9, 2018
Terminated
Nov 14, 2018
Quantity
4,657 cases
Location
Los Angeles, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

Nationwide distribution and Canada

FDA source record · F-0910-2018

Data updated September 16, 2026. View official FDA data ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.