Drug recall
Dr. Pepper Cherry, 12oz (12 pack cans), Manufactured under the authority of Doctor Pepper Company, 5301 Legacy…
FDA recall event 73831 · Class II · The Coca-Cola Company
Key facts
| Event ID | 73831 |
|---|---|
| Recall numbers | F-0561-2017 |
| Recalling firm | The Coca-Cola Company |
| Product type | Food |
| Products | Dr. Pepper Cherry, 12oz (12 pack cans), Manufactured under the authority of Doctor Pepper Company, 5301 Legacy Drive, Plano, TX. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The product contains undeclared High-fructose Corn Syrup (HFCS). |
| Initiation date | Mar 31, 2016 |
| Report date | Dec 14, 2016 |
| Termination date | Dec 5, 2016 |
| City | Atlanta |
| State | GA |
| Country | United States |
| FEI number | 3008016633 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: