FDA-Food2026-03-25Class IIIPROCESSING DEFECT

Winder Laboratories multivitamin with fluoride chewable tablets recalled for low vitamin D

Check Winder Laboratories multivitamin bottles

Winder Laboratories is recalling certain batches of their grape-flavored multivitamin with fluoride chewable tablets because they contain less vitamin D than stated on the label. The FDA discovered this during an inspection. The affected products are the 0.25 mg and 1 mg formulations with specific lot numbers and expiration dates in October and November 2025.

  • Check if you have one of the affected lot numbers (1692303, 1692304, or 1712301) with expiration dates of 10/26/2025 or 11/14/2025.
  • Stop giving the tablets to your child and consult your pediatrician about whether to use an alternative multivitamin.
  • Return the product to the pharmacy or place of purchase for a refund.
Hazard

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

Sold states
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.
Affected count
422cs/12/0.25mg/100ct bottles + 210cs/12/1.0mg/100ct bottles
Manufactured in
716 Patrick Industrial Ln, N/A, Winder, GA, United States
Products
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

Official notice

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=H-0569-2026

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