Home › Recall events › Winder Laboratories, LLC recall — Multivitamin with…
Winder Laboratories, LLC recall — Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC…
FDA (enforcement) · March 25, 2026 · Class III
- Winder Laboratories, LLC recalled Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.25 mg 100… — an FDA enforcement event posted , classified Class III, covering 1 product entry.
- FDA-stated reason: Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
- Details as of ; the linked official notice is authoritative for lot codes, VINs, and remedies.
- Agency
- FDA
- Posted
- Initiated
- Classification
- Class III
- Status
- Ongoing
- Recalling firm
- Winder Laboratories, LLC
- Source ID
- 97884
FDA Enforcement Report search →
Product entries (1)
| Recall # | Product | Codes / lots | Distribution |
|---|---|---|---|
| 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; NDC 75826-171-10 1mg 100 TABLETS UPC 3… | Lot 1692303 SN: 138909557498 EXP: 2025-10-26 & Lot 1692304 SN 131163901709 EXP:… | Product was shipped to the following states: AL, AZ, CA,… |
FDA enforcement entries have no per-recall public URL — verify via the FDA Enforcement Report search using the firm name or a recall number above.
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