Drug recall
Sunkist Orange Soda, 12 fluid oz (355 ml) packaged in PET bottles
FDA recall event 56870 · Class III · Dr. Pepper Snapple Group Inc
Key facts
| Event ID | 56870 |
|---|---|
| Recall numbers | F-0217-2011 |
| Recalling firm | Dr. Pepper Snapple Group Inc |
| Product type | Food |
| Products | Sunkist Orange Soda, 12 fluid oz (355 ml) packaged in PET bottles |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Product was mis-labeled. Caffeine content was indicated at 41 mg, but product contained approximately 238 mg. |
| Initiation date | Sep 28, 2010 |
| Termination date | Feb 28, 2011 |
| City | Plano |
| State | TX |
| Country | United States |
| FEI number | 3004557009 |
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