FDA recall record
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 - 16...
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of November 14, 2018. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
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. , Los Angeles, CA 90021
Reason
Firm was notified by customer of peanut allergen found in the product during product sampling and testing in Kancho Choco Biscuits.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
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. , Los Angeles, CA 90021
Code information listed by FDA
All codes Product ID #: 10142080
Distribution and firm information
Recalling firm listed by FDA: Lotte International America Corp.
Firm location listed by FDA: Los Angeles, CA, United States
Distribution reported by FDA: Nationwide distribution and Canada
Product quantity listed by FDA: 4,657 cases
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.