Refresco Beverages US — FDA Recall History & Enforcement Records
Data Notice: Recall frequency varies by category and firm size; data is comparative and may not indicate actual brand safety or quality. See Methodology.
As of July 16, 2026, Refresco Beverages US has 3 recorded FDA food enforcement actions in the openFDA database. Their most recent recall was on 26 Aug 2024. Refresco Beverages US is categorized under Beverages based on their predominant recall history.
Recall activity over time for Refresco Beverages US
How serious are Refresco Beverages US recalls?
FDA recall classifications by severity
Full FDA recall history for Refresco Beverages US
All 3 FDA enforcement actions sourced from openFDA · Sorted by date, most recent first
| Date | Product | Reason | Class & Status |
|---|---|---|---|
| 26 Aug 2024Official FDA Notice | a.) Great Value 8oz Apple Juice in 6pack; PET plastic bottle b.) Great Value 96oz Apple Juice; PET plastic bottle c.) | Products contains inorganic arsenic above action level set in guidance to industry. | Class IITerminated |
| 15 Aug 2024Official FDA Notice | Great Value; 8oz Apple Juice in 6 pack; 100% Juice; packaged in 8 oz. PET plastic bottles; UPC 0-78742-29655-5 | Product contains inorganic arsenic above action level set in industry guidance (13.2ppb) | Class IITerminated |
| 7 Jul 2022Official FDA Notice | Clear American brand “Strawberry Punch Snow Cone” flavored sparkling water beverage with other natural flavors; 1-liter | The product may contain trace amounts of coconut, which is not declared on the labeling. Laboratory analysis was unable to detect any coconut allergen | Class IITerminated |
Where have Refresco Beverages US recalls occurred?
States affected across all recorded FDA enforcement actions
Where does this recall data come from?
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Data sourced from the FDA Recall Enterprise System via openFDA API. This information is for educational purposes only and does not constitute health or legal advice. FoodRecallFinder.com is not affiliated with or endorsed by the U.S. Food and Drug Administration.
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