Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.25 mg 100 TABLETS
Recalling firm: Winder Laboratories, LLC
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
Check your package
Compare the exact product and package details with the label you have.
FDA code information
Lot 1692303 SN: 138909557498 EXP: 2025-10-26 & Lot 1692304 SN 131163901709 EXP: 2025-10-26; LOT 1712301 SN: 163590222021 EXP: 2025-11-14
Match the product, package size, and code together. A missing match does not guarantee safety.
Full FDA record and distribution details
Original product 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
Original FDA recall reason
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
Recall details
- Recall number
- H-0569-2026
- Event ID
- 97884
- FDA status
- Ongoing
- Initiated
- Oct 27, 2025
- Reported
- Mar 25, 2026
- Classified
- Mar 13, 2026
- Quantity
- 422cs/12/0.25mg/100ct bottles + 210cs/12/1.0mg/100ct bottles
- Location
- Winder, GA, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Letter
Where it was distributed
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.
Data updated September 16, 2026. View official FDA data ↗
Follow official FDA and manufacturer guidance.