Dr — Class III food recall F-1344-2017
Terminated recall by Coca-Cola Consolidated, reported 2017-02-01, distributed in NC. Product labeled Dr. Pepper may instead contain Diet Dr. Pepper (containing undeclared Aspartame as a sweetener
| Recall number | F-1344-2017 |
|---|---|
| Product type | Food |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Coca-Cola Consolidated, Charlotte, NC, United States |
| Recall initiated | 2017-01-05 |
| Classified | 2017-01-25 |
| Reported by FDA | 2017-02-01 |
| Terminated | 2017-01-30 |
| Distributed | NC |
| Reason classes | undeclared allergen, labeling |
Product
Dr. Pepper, 2 Liters (2.1 qt) plastic bottles, Bottled under the authority of Dr. Pepper Company, 5301 Legacy Drive, Plano, TX 75024.
Reason for recall
Product labeled Dr. Pepper may instead contain Diet Dr. Pepper (containing undeclared Aspartame as a sweetener).
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-1344-2017. 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.