Epic Enterprises, Incorporated is recalling 1,703 cases of Dr. Pepper 24-packs of 12 FL OZ cans because the product contains the sweetener aspartame, which is not declared on the label. This recall affects products distributed in Connecticut, Maine, and Rhode Island. Consumers who have these products should return them to the place of purchase for a full refund or dispose of them.
The product contains aspartame, a sweetener that must be declared for individuals with phenylketonuria (PKU), who cannot metabolize the amino acid phenylalanine. Consuming aspartame without awareness poses a health risk to those with this specific metabolic disorder.
You have 2 options:
Produced under the authority of Dr. Pepper/Seven Up, Inc., 5301 Legacy Drive, Plano, TX 75024; Recall #: F-0125-2020
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES ยท Raw API Response
openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.