FDA-Food2026-03-25Class IIIPROCESSING DEFECT
Winder Laboratories multivitamin with fluoride chewable tablets recalled for low vitamin D
What this means
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.
The agency's original wording
Hazard
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
Intended for
Children
Illnesses reported
None reported
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
UPC codes
- 315826169102
- 315826171105
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=H-0569-2026Want us to check the next one for you?
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