FDAFDA · Food and drugs·Recall number 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
Published March 25, 2026 · Recall initiated: October 27, 2025
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Winder Laboratories, LLC
- Distributor
- 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.
- Lot
- Lot 1692303 SN: 138909557498 EXP: 2025-10-26 & Lot 1692304 SN 131163901709 EXP: 2025-10-26; LOT 1712301 SN: 163590222021 EXP: 2025-11-14
- Risk classification
- Class III
- Area (FDA)
- food
- Country
- United States
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