Food recall

Winder Laboratories, LLC recall: Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.25 mg 100 TABLETS UPC 3 15826 16910 2

Winder Laboratories, LLC, of Winder, GA, recalled Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.25 mg 100 TABLETS UPC 3 15826 16910 2. The FDA's reason: “Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.” The FDA classified it Class III: it is unlikely to cause harm. The company began the recall voluntarily on October 27, 2025, and the FDA first listed it in its Enforcement Report of March 25, 2026. The recall is still going on.

How serious

Class III

It is unlikely to cause harm

Why

See FDA's words below

Status

Ongoing

The recall

Company
Winder Laboratories, LLC (Winder, GA)
Reason, in FDA's words
“Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.”
Where it was sold
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.
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
97884

The product recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • H-0569-2026 Class III

    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

    Codes: 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

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of March 25, 2026.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.