Severity
Low
LowClass IIITerminated
FDA Food recall · Reported November 13, 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; Case UPC: 078000082104; Can UPC: 07831504
Product contains undeclared sweetener - aspartame
Compiled from official public sources by the editorial team.
Verify with FDA Food →
Epic Enterprises, Incorporated recalled Dr. Pepper 24 pack of 12 FL OZ Cans (288 FL OZ) in cardboard cases: Produced under the au… - a low-severity action.
Dr. Pepper 24 pack of 12 FL OZ Cans (288 FL OZ) in cardboard cases: Produced under the au… was recalled by Epic Enterprises, Incorporated in November 13, 2019. Reason: Product contains undeclared sweetener - aspartame. Check the official notice for the remedy. Verify recall #F-0125-2020 with the FDA Food before acting.
The recall
Epic Enterprises, Incorporated issued this low-severity FDA Food recall-Product contains undeclared sweetener - aspartame.
- Low
- severity level
- Class III
- classification
- November 13, 2019
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-0125-2020 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-0125-2020) was formally reported on November 13, 2019, with the manufacturer initiating the action on October 16, 2019. It is classified under Low severity (Class III), with a current status of Terminated. Epic Enterprises, Incorporated is listed as the recalling firm, operating out of Ayer, MA. Federal records list the affected scope as 1703 cases.
The documented reason for this recall is: Product contains undeclared sweetener - aspartame Distribution data in the federal record shows the product reached: Products were distributed in CT, ME, RI. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 2 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Food recalls over time
Where this recall sits in its category - 25,126 food recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
1703 cases
Related Recalls
6
2 from same agency
Product description
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
Reason for recall
Product contains undeclared sweetener - aspartame
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | F-0125-2020 |
| Date reported | November 13, 2019 |
| Date initiated | October 16, 2019 |
| Recalling firm | Epic Enterprises, Incorporated |
| Firm location | Ayer, MA |
| Affected scope | 1703 cases |
| Distribution | Products were distributed in CT, ME, RI |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-0125-2020) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Epic Enterprises, Incorporated. Units affected: 1703 cases.
Why was this product recalled? ▼
Product contains undeclared sweetener - aspartame
Which agency issued this recall? ▼
This recall was issued by the FDA Food on November 13, 2019. Severity: Low. Recall number: F-0125-2020.
Where was the recalled product distributed? ▼
Distribution: Products were distributed in CT, ME, RI.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-0125-2020) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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FDA Food Critical
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Compare this recall with Conair Recalls Over One Million Cuisinart Grill Brushes Due… →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported November 13, 2019. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.