Mason Vitamins — 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, Mason Vitamins has 3 recorded FDA food enforcement actions in the openFDA database. Their most recent recall was on 14 Nov 2022. Mason Vitamins is categorized under Supplements & Specialty based on their predominant recall history.
Recall activity over time for Mason Vitamins
How serious are Mason Vitamins recalls?
FDA recall classifications by severity
Full FDA recall history for Mason Vitamins
All 3 FDA enforcement actions sourced from openFDA · Sorted by date, most recent first
| Date | Product | Reason | Class & Status |
|---|---|---|---|
| 14 Nov 2022Official FDA Notice | People’s Choice Women’s Daily Vitamins with Iron, 30 Tablets, Dietary Supplement | Product is sub-potent for Vitamins A, B12, B5 (Pantothenic acid), C, and E not meeting label claims. | Class IIITerminated |
| 14 Nov 2022Official FDA Notice | Healthy Sense Daily Multiple with Iron, Dietary Supplement, 20 Tablets | Product is sub-potent for Vitamins A, B12, B5 (Pantothenic acid), C, and E not meeting label claims. | Class IIITerminated |
| 6 Jul 2015Official FDA Notice | Coenzyme Q-10 50 mg label reads in part, “***Major***CO Q-10 50 MG***For healthy HEART & IMMUNE function***Promotes ENER | Product is mislabeled. Some of the Co Q 10 30 mg bottles were labeled with the incorrect label, Co Q 10 50 mg. | Class IIITerminated |
Where have Mason Vitamins 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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