Epic Enterprises, Incorporated recalls Dr. Pepper 24 pack of 12 FL OZ Cans (288 FL OZ) in cardboard cases: Produced under the authority of Dr. Pepper/Seven
Dr. Pepper 24-pack of 12 fl oz cans (288 fl oz) recalled due to undeclared sweetener aspartame. Check UPCs: 078000082104 (case) and 07831504 (can).
Lower-risk recall
Product contains undeclared sweetener - aspartame
Contact the company & request your remedy
What happened, in plain English
Dr. Pepper 24-packs of 12 fl oz cans (288 fl oz) in cardboard cases are being recalled because they contain aspartame, a sweetener not declared on the label. This could pose a risk for people with diabetes or other health conditions that require careful monitoring of sweetener intake. Read more at govinfonow.com/recall/16500-dr-pepper-24-pack-recall-undeclared-aspartame-in-cans.
Source Summary by GovInfoNow · govinfonow.com/recall/16500-dr-pepper-24-pack-recall-undeclared-aspartame-in-cans · Updated October 5, 2026 · FDA enforcement record: FDA #F-0125-2020
Cite this page
“Dr. Pepper 24-Pack Recall: Undeclared Aspartame in Cans.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/16500-dr-pepper-24-pack-recall-undeclared-aspartame-in-cans. Based on FDA recall #F-0125-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0125-2020%22&limit=1).
Why it’s dangerous
The product contains aspartame, a sweetener that is not listed on the label. Aspartame is a dipeptide that can cause health issues for some individuals, particularly those with diabetes or other conditions requiring strict sweetener monitoring.
Who’s affected
People who purchased Dr. Pepper 24-packs of 12 fl oz cans with the specific UPC codes listed in the recall notice are affected. Those with diabetes or other health conditions sensitive to aspartame are at higher risk.
How to tell if you have this one
Check for the case UPC 078000082104 and can UPC 07831504 on the cardboard case and individual cans. The recall covers Dr. Pepper 24-packs produced with the case lot number XXXXEA09239CD and can lot number XXXXEA09239C.
- Brand
Dr. Pepper- Product
Dr. Pepper 24 pack of 12 FL OZ Cans (288 FL OZ) in cardboard cases: Produced under the authority of Dr. Pepper/Seven- Category
Food
What to do — step by step
Check Product UPCs
Look for case UPC 078000082104 and can UPC 07831504 on the cardboard case and individual cans.
Questions people ask
Why is this product being recalled?
The product contains aspartame, a sweetener not declared on the label, which could pose a risk for people with diabetes or other health conditions requiring careful sweetener monitoring.
How do I know if I have the recalled product?
Check for case UPC 078000082104 and can UPC 07831504 on the cardboard case and individual cans. The recall covers Dr. Pepper 24-packs produced with the case lot number XXXXEA09239CD and can lot number XXXXEA09239C.
What should I do if I have the recalled product?
The recall does not specify a remedy, so contact Epic Enterprises, Incorporated for further instructions.
Contact Dr. Pepper
We’ve drafted a message you can send Dr. Pepper to request your refund or repair — edit it as you like.
Subject: Recall F-0125-2020 — Dr. Pepper Dr. Pepper 24 pack of 12 FL OZ Cans (288 FL OZ) in cardboard cases: Produced under the a Hello, I own a Dr. Pepper 24 pack of 12 FL OZ Cans (288 FL OZ) in cardboard cases: Produced under the authority of Dr. Pepper/Seven that is covered by recall F-0125-2020 from Dr. Pepper. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-0125-2020 (October 16, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0125-2020 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.