Recall Radar

Epic Enterprises recalls Dr. Pepper: allergen risk

November 13, 2019 · Epic Enterprises Class III

Class IIIFDA’s lowest-risk class: use of the product is not likely to cause adverse health consequences.
Reason for the recallProduct contains undeclared sweetener - aspartame

Find the official FDA enforcement report

Recall at a glance

Recalling company
Epic Enterprises
Location
Ayer, MA
Reported by FDA
November 13, 2019
Recall started
October 16, 2019
Risk class
Class III
Status (latest data we have)
Terminated
Type
Voluntary: Firm initiated
Category
Fresh produce
Reason type
Undeclared allergens

Is my product affected?

Compare your product’s name, size and lot or date codes with the list below. A recall usually covers only specific codes.

  • 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
    Quantity: 1703 cases
    Codes: 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

Where it was distributed

Products were distributed in CT, ME, RI

What to do

If you have this product, check the codes above. FDA recall notices often tell consumers to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information, and if you are unsure, do not eat it. If someone becomes ill after eating a recalled food, contact a healthcare professional. See FDA’s recalls and safety alerts for company announcements.

Frequently asked questions

What was recalled?

Epic Enterprises recalled 1 product, including 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….

Why was it recalled?

Product contains undeclared sweetener - aspartame

What does Class III mean?

FDA’s lowest-risk class: use of the product is not likely to cause adverse health consequences.

Where was it sold or shipped?

Products were distributed in CT, ME, RI

What should I do if I have this product?

Compare the product name, size and lot or date codes with the details on this page. FDA recall notices often tell you to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information. If you are unsure, do not eat it.

Similar recalls in fresh produce

Sources

Data provided by the U.S. Food and Drug Administration (FDA) through openFDA, shown as published and not validated by this site. This site is independent and is not affiliated with or endorsed by FDA. It covers FDA-regulated foods; meat, poultry and egg products are regulated by USDA. Do not rely on this site for medical decisions: for health concerns contact a healthcare professional, and always follow the official notice and the company’s instructions. Terms and disclaimer.