Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 758…

Winder Laboratories, LLC has recalled Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 758…, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on March 25, 2026 and was initiated on October 27, 2025. It is classified as a Class III recall, which means using this product is not likely to cause health problems, but it breaks an FDA rule (for example, a labeling or packaging issue).

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 758…, with approximately 422cs/12/0.25mg/100ct bottles + 210cs/12/1.0mg/100ct bottles affected. The company behind the recall is Winder Laboratories, LLC, based in Winder, GA. The FDA describes the product as: “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”

Why was Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 758… recalled?

According to the FDA, the stated reason for the recall is: “Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.” In plain terms, this recall relates to a potency or effectiveness issue.

This recall means the medicine may be stronger or weaker than its label says, or may not release its ingredient the way it should. That matters because too little medicine may not treat the condition, and too much can cause side effects. Anyone taking an affected product is generally advised to consult their pharmacist or doctor about a replacement.

What should you do?

If you think you may have bought Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 758…, compare it against the product description and identifying codes (Lot 1692303 SN: 138909557498 EXP: 2025-10-26 & Lot 1692304 SN 131163901709 EXP: 2025-10-26; LOT 1712301 SN: 163590222021 EXP: 2025-11-14) before using it. This recall is currently listed as ongoing.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Winder Laboratories, LLC or your local health authority.

About this recall

This recall was distributed in GA. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.