Winder Laboratories fluoride multivitamin recalled for low vitamin D
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.
From the FDA notice · Read the official notice ↗
What to do
- 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.
Is yours affected?
Compare your label or packaging with the recalled product.
- Product
- 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
- Sold in
- 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.
- Made for
- Children
Details
- Units affected
- 422cs/12/0.25mg/100ct bottles + 210cs/12/1.0mg/100ct bottles
- Illnesses reported
- None reported
- Manufactured in
- 716 Patrick Industrial Ln, N/A, Winder, GA, United States
- Classification
- Class III
- Recall number
- H-0569-2026
In the FDA's words
- Description
- 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 Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D. Lot 1692303 SN: 138909557498 EXP: 2025-10-26 & Lot 1692304 SN 131163901709 EXP: 2025-10-26; LOT 1712301 SN: 163590222021 EXP: 2025-11-14 Distribution: 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 quantity: 422cs/12/0.25mg/100ct bottles + 210cs/12/1.0mg/100ct bottles
- Hazard
- Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.