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
- FDA Food
- Class III
- ongoing
- Published 2026-03-25
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
| Agency | FDA Food |
|---|---|
| Recall number | H-0569-2026 |
| Classification | Class III |
| Status | ongoing |
| Initiated | 2025-10-27 |
| Published | 2026-03-25 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Winder Laboratories |
| Distribution | 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 |
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
| upc | 315826169102 |
|---|---|
| upc | 315826171105 |
| 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 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: ongoing.
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Source
Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0569-2026%22
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