RecallRadar

FDA Food recall H-0569-2026

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

On 2026-03-25 the FDA classified a Class III recall of Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.25 mg 100 TABLETS UPC 3 15826 16910 2 by Winder Laboratories, citing subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.

Read the official FDA Food notice

AgencyFDA Food
Recall numberH-0569-2026
ClassificationClass III
Statusongoing
Initiated2025-10-27
Published2026-03-25
Last updated2026-09-13 11:51 UTC
CompanyWinder Laboratories
DistributionAL, AZ, CA, FL, HI, IA, IL, IN, MA, MI, MO, MS, NC, NJ, NY, OR, PA, PR, RI, TN, TX, UT, WA, WI, WV

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

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

Identifiers

upc315826169102
upc315826171105
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

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0569-2026%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.