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Winder Laboratories, LLC
FDA recall H-0569-2026 · Class III · reported 2026-03-25 · Ongoing
- Product
- 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
- Reason
- Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
- Quantity
- 422cs/12/0.25mg/100ct bottles + 210cs/12/1.0mg/100ct bottles
- 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.
- Firm location
- GA, United States
- Initiated
- Voluntary: Firm initiated
- First notice
- Letter
- Recall started
- 2025-10-27
- 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: U.S. Food and Drug Administration, openFDA Food Enforcement database (openFDA Food Enforcement, imported 2026-09). The FDA does not validate openFDA data for completeness or accuracy. This is a record of an enforcement action, not safety advice.