Winder Laboratories, LLC is recalling 632 cases of Multivitamin with Fluoride Chewable Tablets because an FDA inspection found the product is subpotent for Vitamin D. This means the tablets do not contain the full amount of Vitamin D listed on the label. If you have health concerns regarding this subpotency, you should contact your healthcare provider or pharmacist.
The product was found to be subpotent for Vitamin D during an FDA inspection, meaning users may not receive the intended nutritional or therapeutic benefit of the vitamin supplement.
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Recall #: H-0569-2026; Quantity: 422cs of 0.25mg and 210cs of 1.0mg
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Sources: FDA iRES · Raw API Response
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