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…
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
What to do
- 1Compare your lot code with the recall details.
- 2Do not use the item if your lot is listed.
- 3Return it if the store accepts recalled products.
Recall details
- Firm
- Winder Laboratories, LLC
- Status
- Ongoing
- Reported
- Mar 25, 2026
- Started
- Oct 27, 2025
- Where 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.
- Quantity
- 422cs/12/0.25mg/100ct bottles + 210cs/12/1.0mg/100ct bottles
- FDA number
- H-0569-2026
Lots, UPC, dates
Lot 1692303 SN: 138909557498 EXP: 2025-10-26 & Lot 1692304 SN 131163901709 EXP: 2025-10-26; LOT 1712301 SN: 163590222021 EXP: 2025-11-14
FDA wording
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
Source: FDA report. This is not medical advice. Compare your package codes before you act.