Valley Springs Artesian Gold — 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, Valley Springs Artesian Gold has 3 recorded FDA food enforcement actions in the openFDA database. Their most recent recall was on 6 Feb 2026. Valley Springs Artesian Gold is categorized under Beverages based on their predominant recall history.
Recall activity over time for Valley Springs Artesian Gold
How serious are Valley Springs Artesian Gold recalls?
FDA recall classifications by severity
Full FDA recall history for Valley Springs Artesian Gold
All 3 FDA enforcement actions sourced from openFDA · Sorted by date, most recent first
| Date | Product | Reason | Class & Status |
|---|---|---|---|
| 6 Feb 2026Official FDA Notice | Valley Springs 100% Natural Bottled Water. Fluoride Added. 1 Gal Net, 128 Fl. Oz. UPC 0 31193-01301 0. Bottled by Va | Water was bottled under insanitary conditions. | Class IIOngoing |
| 6 Feb 2026Official FDA Notice | Valley Springs Steamed Distilled Water. 1 Gal Net, 128 Fl. Oz. UPC 0 31193-00601 2. Bottled by Valley Springs/Artesia | Water was bottled under insanitary conditions. | Class IIOngoing |
| 6 Feb 2026Official FDA Notice | Valley Springs 100% Natural Bottled Water packaged in the following size plastic jug with plastic caps: 1. 1 Gal Net | Water was bottled under insanitary conditions. | Class IIOngoing |
Where have Valley Springs Artesian Gold 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.
To determine if your specific product is affected, verify that the brand name, product description, lot number, UPC code, and date range all match the recall details exactly. When in doubt contact the recalling firm or visit FDA.gov.
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