Class IIITerminated in FDA datasetOct 16, 2019

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;…

Recalling firm: Epic Enterprises, Incorporated

Why it was recalled

Product contains undeclared sweetener - aspartame

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The exact product

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

Check the codes

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

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Original FDA code information

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

TypeCode / valueContext
UPC078000082104Up, Inc., 5301 Legacy Drive, Plano, TX 75024; Best Before: JUN 29 20; Case UPC: 078000082104; Can UPC: 07831504

Recall details

Recall number
F-0125-2020
Event ID
84069
FDA status
Terminated
Initiated
Oct 16, 2019
Reported
Nov 13, 2019
Classified
Nov 6, 2019
Terminated
Dec 18, 2019
Quantity
1703 cases
Location
Ayer, MA, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Products were distributed in CT, ME, RI

FDA source record · F-0125-2020

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.