Home/Recalls/FDA-H-0569-2026
FDA FoodClass III

Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.2...

Published: March 25, 2026Recall ID: H-0569-2026Category: foodCountry: US

Reason for Recall / Hazard

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

Product Description & Identification

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

Additional Source Details

FieldValue
CityWinder
StateGA
Event id97884
Address 1716 Patrick Industrial Ln
Address 2N/A
Code infoLot 1692303 SN: 138909557498 EXP: 2025-10-26 & Lot 1692304 SN 131163901709 EXP: 2025-10-26; LOT 1712301 SN: 163590222021 EXP: 2025-11-14
Postal code30680-8333
Report date20260325
Product typeFood
Product quantity422cs/12/0.25mg/100ct bottles + 210cs/12/1.0mg/100ct bottles
Reason for recallSubpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20251027
Initial firm notificationLetter
Center classification date20260313

Overview

  • Recalling FirmWinder Laboratories, LLC
  • StatusOngoing
  • Risk LevelClass III
  • DistributionProduct 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.
Official Agency Alert