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Class I: serious health riskTerminated

Lotte Kancho Choco-Biscuit Recall

Lotte Kancho Choco-Biscuit

Lotte International America Corp. · Los Angeles, CA

Risk level
Class I
Reported by FDA
Mar 14, 2018
Recall ID
F-0910-2018
Check your lot numberHow we source this data

Summary

Lotte International America recalled Lotte Kancho Choco-Biscuit starting Feb 20, 2018. The FDA classified it as Class I (serious health risk) and published enforcement report F-0910-2018 on Mar 14, 2018. Reason: Firm was notified by customer of peanut allergen found in the product during product sampling and testing in Kancho Choco Biscuits. Status: Terminated.

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.

Product description

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

Lot numbers, UPCs & expiration codes

All codes Product ID #: 10142080

Where it was sold

Nationwide distribution and Canada

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-0910-2018
Classification
Class I
Status
Terminated
Recall initiated
Feb 20, 2018
FDA report date
Mar 14, 2018
Quantity
4,657 cases
Recall type
Voluntary: Firm initiated
Recalling firm
Lotte International America Corp.

Original FDA data

Every field from FDA enforcement report F-0910-2018, exactly as published.

Show all FDA fields
City
Los Angeles
State
CA
Status
Terminated
Country
United States
Event ID
79312
Address
1805 Industrial St
Code information
All codes Product ID #: 10142080
Postal code
90021-1223
Report date
Mar 14, 2018
Product type
Food
Recall number
F-0910-2018
Classification
Class I
Recalling firm
Lotte International America Corp.
Product quantity
4,657 cases
Termination date
Nov 14, 2018
Reason for recall
Firm was notified by customer of peanut allergen found in the product during product sampling and testing in Kancho Choco Biscuits.
Voluntary / mandated
Voluntary: Firm initiated
Product description
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
Distribution pattern
Nationwide distribution and Canada
Recall initiation date
Feb 20, 2018
Initial firm notification
Letter
Center classification date
Mar 9, 2018

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0910-2018, published Mar 14, 2018. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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