Recalls / Class III

Class IIIH-0569-2026

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

Type

Food

Affected lot / 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

Quantity

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

Why it was recalled

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

Recalling firm

Firm

Winder Laboratories, LLC

Notification channel

Letter

Type

Voluntary: Firm initiated

Address

716 Patrick Industrial Ln, N/A, Winder, Georgia 30680-8333

Distribution

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.

Timeline

Recall initiated

2025-10-27

FDA classified

2026-03-13

Posted by FDA

2026-03-25

Status

Ongoing

Source: openFDA Food Enforcement endpoint. Recall record H-0569-2026. The FDA issues recall classifications as health-hazard assessments, not legal findings.