WhichRecall
Class IIIReported 2026-03-25

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

Recalled by Winder Laboratories, LLC

Reason for Recall

Subpotent

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During an FDA inspection it was discovered that the product was subpotent for Vitamin D.

Recall Number
H-0569-2026
Classification
Class III
Status
Ongoing
Category
food
Initiated
2025-10-27
Reported
2026-03-25
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.
Code Info
Lot 1692303 SN: 138909557498 EXP: 2025-10-26 & Lot 1692304 SN 131163901709 EXP: 2025-10-26; LOT 1712301 SN: 163590222021 EXP: 2025-11-14
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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