Home / Recalls / Winder Laboratories, LLC / H-0569-2026

H-0569-2026 Class III Ongoing

Recalled by Winder Laboratories, LLC — Winder, GA

Recall Details

Product Type: Food
Report Date: March 25, 2026
Initiation Date: October 27, 2025
Termination Date: N/A
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 422cs/12/0.25mg/100ct bottles + 210cs/12/1.0mg/100ct bottles

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

Reason for Recall

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

Distribution Pattern

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 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