Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC… — Class III food recall H-0569-2026
Ongoing recall by Winder Laboratories, LLC, reported 2026-03-25, distributed in AL, AZ, CA, FL, HI, IA, IL, IN…. Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
| Recall number | H-0569-2026 |
|---|---|
| Product type | Food |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Winder Laboratories, LLC, Winder, GA, United States |
| Recall initiated | 2025-10-27 |
| Classified | 2026-03-13 |
| Reported by FDA | 2026-03-25 |
| Distributed | 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 |
| Reason classes | potency |
| NDC | 75826-0169-10, 75826-0171-10 |
| Lot numbers | 131163901709, 138909557498, 163590222021, 1692303, 1692304, 1712301 |
| Expiration dates | 2025-10-26, 2025-11-14 |
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 for recall
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/H-0569-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.