Lotte International America Corp. Recall: Firm was notified by customer of peanut allergen found in the product during product sampling and testing in Kancho Choco Biscuits. - F-0910-2018
United States
TerminatedClass I
- Company
- Lotte International America Corp.
- Product
- Lotte Kancho Choco-Biscuit; Sold as Lotte Kancho - 42 g…
- Recall date
- February 20, 2018
- Terminated
- November 14, 2018
- Source
- FDA
Reason for recall
Firm was notified by customer of peanut allergen found in the product during product sampling and testing in Kancho Choco Biscuits.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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 | Not published in this source record | 4,657 cases | All codes Product ID #: 10142080 |
Distribution
- Nationwide distribution and Canada
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0910-2018
- Event ID
- 79312
- Status
- Terminated
- Classification
- Class I
- Company
- Lotte International America Corp.
- 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
- Quantity
- 4,657 cases
- Reason
- Firm was notified by customer of peanut allergen found in the product during product sampling and testing in Kancho Choco Biscuits.
- Recall initiation date
- February 20, 2018
- Report date
- March 14, 2018
- Classification date
- Not published in this source record
- Termination date
- November 14, 2018
- Distribution pattern
- Nationwide distribution and Canada
- UPC, lot, and code information
- All codes Product ID #: 10142080
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Letter
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Lotte International America Corp.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
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Technical source data
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Frequently asked questions
What does a Class I mean?
FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
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Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Official guidance and record verification
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How to interpret this historical record
This record is preserved as published by FDA, as of November 14, 2018.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
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