FDA recall record
Dr. Pepper 24 pack of 12 FL OZ Cans (288 FL OZ) in cardboard cases: Produced under the authority of Dr. Pepper/Seven Up, Inc., 5301 Legacy Drive, Plano, TX 75024; Best Before: J...
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 December 18, 2019. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Dr. Pepper 24 pack of 12 FL OZ Cans (288 FL OZ) in cardboard cases: Produced under the authority of Dr. Pepper/Seven Up, Inc., 5301 Legacy Drive, Plano, TX 75024; Best Before: JUN 29 20; Case UPC: 078000082104; Can UPC: 07831504
Reason
Product contains undeclared sweetener - aspartame
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.
Dr. Pepper 24 pack of 12 FL OZ Cans (288 FL OZ) in cardboard cases: Produced under the authority of Dr. Pepper/Seven Up, Inc., 5301 Legacy Drive, Plano, TX 75024; Best Before: JUN 29 20; Case UPC: 078000082104; Can UPC: 07831504
Code information listed by FDA
Outer wrap Dates: Ship To Satelite 03/09/2020; Ship To Trade 05/18/2020; Best Taste Before 06/29/2020 Case date: JUN 29 20 Case Lot: XXXXEA09239CD Can date: JUN 29 20 Can Lot: XXXXEA09239C
Distribution and firm information
Recalling firm listed by FDA: Epic Enterprises, Incorporated
Firm location listed by FDA: Ayer, MA, United States
Distribution reported by FDA: Products were distributed in CT, ME, RI
Product quantity listed by FDA: 1703 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.