Dr — Class III food recall F-0125-2020
Terminated recall by Epic Enterprises, Incorporated, reported 2019-11-13, distributed in CT, ME, RI. Product contains undeclared sweetener - aspartame
| Recall number | F-0125-2020 |
|---|---|
| Product type | Food |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Epic Enterprises, Incorporated, Ayer, MA, United States |
| Recall initiated | 2019-10-16 |
| Classified | 2019-11-06 |
| Reported by FDA | 2019-11-13 |
| Terminated | 2019-12-18 |
| Distributed | CT, ME, RI |
| Quantity | 1,703 cases |
| Reason classes | undeclared allergen |
| UPC / GTIN / UDI-DI | 00078000003154, 00078000082104 |
| Lot numbers | XXXXEA09239C, XXXXEA09239CD |
Product
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-0125-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.