Information
Winder Laboratories Recalls Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx
This is a Class III recall. This product is unlikely to cause adverse health reactions but violates FDA regulations.
Source: FDA
InfoRecall #H-0569-2026Food
Winder Laboratories Recalls Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx
Winder Laboratories, LLC · Class III — Regulatory
Product Description
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 100 TABLETS UPC 3 15826 17110 5 Manufactured by: WINDER LABORATORIES LLC Winder, GA 30680
Reason for Recall
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
FDA Classification
Class III — Regulatory
A situation in which use of, or exposure to, a violative product is not likely to cause adverse health consequences.
Distribution
Product was shipped to the following states: AL, AZ, CA, FL, HI, IA, IL, IN, MA, MI, MO, MS, NC, NJ, NY, OR, PA, PR, RI, TN, TX, UT, WA, WI & WV.
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
Winder Laboratories, LLC initiated a Class III recall of a food product on October 27, 2025 affecting 422cs/12/0.25mg/100ct bottles + 210cs/12/1.0mg/100ct bottles. Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D. Class III recalls involve products that are unlikely to cause adverse health reactions but violate FDA regulations. The product was distributed nationwide. Consumers may continue monitoring FDA updates regarding this recall.
Sources: FDA openFDA Enforcement Database
This recall appears in: Other Injury Hazards.