Wellements — 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, Wellements has 3 recorded FDA food enforcement actions in the openFDA database. Their most recent recall was on 24 Jul 2020. Wellements is categorized under Supplements & Specialty based on their predominant recall history.
Recall activity over time for Wellements
How serious are Wellements recalls?
FDA recall classifications by severity
Full FDA recall history for Wellements
All 3 FDA enforcement actions sourced from openFDA · Sorted by date, most recent first
| Date | Product | Reason | Class & Status |
|---|---|---|---|
| 24 Jul 2020Official FDA Notice | Iron Drops (UPC 729609000098) liquid Dietary Supplement, 1 oz/30 mL amber glass bottle packaged in an individual product | Product contains undeclared milk | Class ITerminated |
| 24 Jul 2020Official FDA Notice | Iron Drops Sampler (UPC 729609000098) liquid Dietary Supplement, 1 oz/30 mL, (2 mL fill) amber glass bottle packaged in | Product contains undeclared milk | Class ITerminated |
| 18 Jul 2012Official FDA Notice | Wellements Baby Move Prune Concentrate with Prebiotics, 4oz., 12 units per case, SKU# 141161, UPC 729609019878. | Wellements is recalling Wellements Baby Move Prune Concentrate, 4oz. because they have confirmed that their supplier of the ingredient galacto-oligosa | Class ITerminated |
Where have Wellements 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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