Winder Laboratories, LLC recalls Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.25 mg 100 TABLETS UPC 3 15826 16910 2; N…
- Recall date
- October 27, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- H-0569-2026
- FDA classification
- Class III
- Brand / firm
- Winder Laboratories, LLC
- Sold / 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.
Why it was recalled
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
Class III means the product violates regulations but is not likely to cause harm.
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
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