Recall · openFDA Food Enforcement

Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx…: FDA Recall H-0569-2026

Agency action: Oct 27, 2025Record ID: H-0569-2026
View official source ↗

What happened

Original notice title

Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.25 mg 100 TABLETS UPC 3 15826 16910 2, recall H-0569-2026

From the archived source record

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

What the official notice says to do

Check the original notice for the instructions that apply to the named product, company, and affected lots.

Read the official notice →

Status and source details

Status recorded in the archive
Ongoing
FDA recall classification
Class III
Recall initiated by
Voluntary: Firm initiated
Report date
Mar 25, 2026
Source checked
Jul 16, 2026
Record revision
ef46557e070f

This is a dated record. Its current status may have changed since the source was captured. A record applies to its stated scope; it is not a safety rating for every product from a company.

Sources, dates, and coverage →

What is affected

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
Company
Winder Laboratories, LLC
Lot / identifier
Lot 1692303 SN: 138909557498 EXP: 2025-10-26 & Lot 1692304 SN 131163901709 EXP: 2025-10-26; LOT 1712301 SN: 163590222021 EXP: 2025-11-14
Market / 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.