LOW RISK Ongoing H-0569-2026

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

Classification

Class III — Products that are unlikely to cause any adverse health reaction, but that violate FDA labeling or manufacturing laws.

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

Product Quantity

422cs/12/0.25mg/100ct bottles + 210cs/12/1.0mg/100ct bottles

Product Type

Food

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

Voluntary/Mandated

Voluntary: Firm initiated

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.

Company Location

Winder, GA, 30680-8333

Report Date

03/25/2026

Recall Initiated

10/27/2025

Classification Date

03/13/2026

Termination Date

N/A

Source: U.S. Food & Drug Administration (FDA) — FDA Recalls

Last updated: August 28, 2026

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