FDA recall H-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

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

Status

Ongoing

Initiation date

2025-10-27

Report date

2026-03-25

Voluntary/Mandated

Voluntary: Firm initiated

Location

Winder, GA, United States

Primary source

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