# FDA recall H-0569-2026

> **Winder Laboratories, LLC** · Class III · food recall initiated 2025-10-27.

## 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 for recall

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

## 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.

## Key facts

- **Recall number:** H-0569-2026
- **Recalling firm:** Winder Laboratories, LLC
- **Classification:** Class III
- **Product type:** food
- **Status:** Ongoing
- **Initiation date:** 2025-10-27
- **Report date:** 2026-03-25

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Winder, GA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=H-0569-2026

## Citation

> AI Analytics. FDA recall H-0569-2026. Retrieved 2026-09-21 from https://api.ai-analytics.org/recall/H-0569-2026. Source: US FDA. Licensed CC0.

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