Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC… recall
Recalled by Winder Laboratories, LLC · Winder, GA, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
See the recall's own reason text for the specifics. All other reasons recalls.
What was recalled
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
Quantity: 422cs/12/0.25mg/100ct bottles + 210cs/12/1.0mg/100ct bottles
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot 1692303 SN: 138909557498 EXP: 2025-10-26 & Lot 1692304 SN 131163901709 EXP: 2025-10-26; LOT 1712301 SN: 163590222021 EXP: 2025-11-14
Where it was sold
Alabama Arizona California Florida Hawaii Iowa Illinois Indiana Massachusetts Michigan Missouri Mississippi North Carolina New Jersey New York Oregon Pennsylvania Puerto Rico Rhode Island Tennessee Texas Utah Washington Wisconsin West Virginia
FDA's distribution note: 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.
Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it.
- Recalling firm
- Winder Laboratories, LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Oct 27, 2025
- In FDA report of
- Mar 25, 2026
- FDA recall number
- H-0569-2026 · event 97884
- Official record
- FDA enforcement report search