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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Low RiskFDA Food
Food & Beverages/Beverages

Dr. Pepper 24-Pack Cans Recalled for Undeclared Aspartame

Agency Publication Date: November 6, 2019
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Summary

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.

Risk

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.

What You Should Do

  1. Check your Dr. Pepper 24-pack cardboard cases for the following identifiers: Case UPC 078000082104, Case Lot XXXXEA09239CD, and a Best Before date of JUN 29 20.
  2. Check individual 12 FL OZ cans for Can UPC 07831504, Can Lot XXXXEA09239C, and a date of JUN 29 20.
  3. Verify the outer wrap dates, which may include 'Ship To Satelite 03/09/2020', 'Ship To Trade 05/18/2020', or 'Best Taste Before 06/29/2020'.
  4. Return the product to the place of purchase for a full refund, throw it away, or contact Epic Enterprises, Incorporated for further instructions.
  5. Call the FDA Consumer Complaint hotline at 1-888-723-3332 for additional questions regarding this recall.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Dr. Pepper 24 pack of 12 FL OZ Cans (288 FL OZ) in cardboard casesby Dr. Pepper
Variants: 12 FL OZ Cans, 24-pack
UPC Codes:
078000082104
07831504
Lot Numbers:
XXXXEA09239CD
XXXXEA09239C
Date Ranges: Best Before: JUN 29 20, Ship To Satelite 03/09/2020, Ship To Trade 05/18/2020, Best Taste Before 06/29/2020

Produced under the authority of Dr. Pepper/Seven Up, Inc., 5301 Legacy Drive, Plano, TX 75024; Recall #: F-0125-2020

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 84069
Status: Resolved
Manufacturer: Epic Enterprises, Incorporated
Sold By: Retailers in CT, ME, and RI
Manufactured In: United States
Units Affected: 1703 cases
Distributed To: Connecticut, Maine, Rhode Island

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.