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

Recall map → All recalls → H-0569-2026

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 Winder Laboratories, LLC · reported 2026-03-25

Ongoing The agency has not recorded this recall as closed out.

Reason for recall: Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
Classification: Class III
Recall initiated: 2025-10-27
Reported by the agency: 2026-03-25
Closed out (terminated): not reported
Recalling firm: Winder Laboratories, LLC
Winder, GA
United States
This is the firm that issued the recall — commonly a distributor or processor. It is not the origin of contamination.
Distribution (the agency's own words): 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.
States we parsed from that text: 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
The agency named these states. Parse method explicit_state_list, confidence high.
Food category: Dietary supplements Produce (fruit & vegetables)derived
Assigned by a reviewed keyword rulebook over the product description, not by the agency.
Recall type: Voluntary: Firm initiated
Recall number: H-0569-2026

This page reproduces a record published by the US Food and Drug Administration. It is not real-time: recalls typically appear in FDA's Enforcement Report weeks after they begin — a median of 40 days, see publication lag. For current food safety information consult FDA and USDA FSIS directly.