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Low risk Dietary SupplementsClass III

Winder Multivitamin Fluoride Chewable Recall

Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.25 mg 100 TABLETS UPC 3 15826 16910 2; NDC 75826-171-10 1mg 1

Updated October 27, 2025

Winder Laboratories is recalling Multivitamin with Fluoride Chewable Tablets in grape flavor because the product contains less Vitamin D than labeled. While this means the tablets may not provide the intended vitamin benefit, there is no immediate safety hazard.

Is the Winder Laboratories, LLC recalled? Yes. This product was recalled by FDA on October 27, 2025. Details below.

What is recalled

Multivitamin with Fluoride Chewable Tablets, Grape Flavor, manufactured by Winder Laboratories LLC (Winder, GA 30680). Two strengths are recalled: 0.25 mg tablets, NDC 75826-169-10, UPC 3 15826 16910 2, 100-tablet bottles; and 1 mg tablets, NDC 75826-171-10, UPC 3 15826 17110 5, 100-tablet bottles.

Am I affected

You're affected if you have Winder Multivitamin with Fluoride Chewable Tablets in grape flavor. Check the bottle label for NDC 75826-169-10 (0.25 mg) or NDC 75826-171-10 (1 mg), or the UPC code 3 15826 16910 2 or 3 15826 17110 5.

What to do right now

Stop using this product. Contact Winder Laboratories, LLC or the retailer where you purchased it to discuss next steps, such as a refund or replacement.

The hazard

Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.

Brands affected

Winder Laboratories, LLC
Source
FDA
Category
Dietary Supplements
Recall ID
fda-H-0569-2026
Classification
Class III
Recalled
October 27, 2025
Read the official notice

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