United StatesMultivitamin with Fluoride Chewable Tablets, Grape Flavor Rx in 0.25 mg (NDC 75826-169-10, UPC 3 15826 16910 2) and 1 mg (NDC 75826-171-10, UPC 3 15826 17110 5), 100‑tablet bottles, lots 1692303, 1692304 and 1712301, manufactured by Winder Laboratories, LLC. The FDA found the product was subpotent for Vitamin D. The recall is ongoing; the product was shipped to multiple U.S. states including AL, AZ, CA, FL, HI, IA, IL, IN, MA, MI, MO, MS, NC, NJ, NY, OR, PA, PR, RI, TN, TX, UT, WA, WI and WV.
What's being recalled
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
Recalling firm: Winder Laboratories, LLC, Winder, GA, United States.
How to identify it
Lot 1692303 SN: 138909557498 EXP: 2025-10-26 & Lot 1692304 SN 131163901709 EXP: 2025-10-26; LOT 1712301 SN: 163590222021 EXP: 2025-11-14
The hazard
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
What to do
Don't eat it. Return it to the store for a refund or throw it away. If you've eaten it and feel unwell, contact a doctor.
The notice doesn't give instructions for consumers, so this is general advice for food & drink recalls. Check the official notice for the details.
Where it was sold
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.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)
