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Food FDA Class III Ongoing Quality

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

Winder Laboratories, LLC Published Mar 25, 2026

Risk level

Class III

Unlikely to cause harm, but violates labeling or manufacturing rules.

Severity score 35/100

What should you do?

  • Check whether you have this product, using the lot codes, UPCs, and dates listed below.
  • Do not eat, serve, or sell the affected product.
  • Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
  • Contact Winder Laboratories, LLC or your place of purchase with questions, and see the source record below for full details.
Reason for recall

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

Affected products (1)

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

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

Lot codes: 1692303, 1692304, 1712301
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

Affected areas

AlabamaArizonaCaliforniaFloridaHawaiiIllinoisIndianaIowaMassachusettsMichiganMississippiMissouriNew JerseyNew YorkNorth CarolinaOregonPennsylvaniaPuerto RicoRhode IslandTennesseeTexasUtahWashingtonWest VirginiaWisconsin

Timeline

  1. Initiated
    Oct 27, 2025
  2. Published
    Mar 25, 2026
Recall number
H-0569-2026
Agency
U.S. Food and Drug Administration
Country
US
Source data (openFDA JSON) About FDA enforcement reports

FDA records come from the openFDA food enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.