Use caution Food recall · FDA · Published October 27, 2025

Winder Labs Recalls Grape Multivitamins Due to Subpotent Vitamin D

Winder Laboratories recalls specific lots of grape-flavored chewable multivitamins because they contain less than labeled amounts of Vitamin D.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #H-0569-2026Food Winder Laboratories ›

Use caution until it’s fixed

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

Take action

Contact the company

Recalling firmWinder Laboratories, LLC716 Patrick Industrial Ln · Winder, GA 30680-8333

✎ GovInfoNow plain-language explainer

Winder Laboratories, LLC is recalling Multivitamin with Fluoride Chewable Tablets in Grape Flavor due to a manufacturing error that resulted in subpotent Vitamin D levels. The product was identified as deficient during an FDA inspection. Consumers who purchased the affected lots should check their bottles against the specific lot numbers and serial numbers listed below. Read more at govinfonow.com/recall/7044-winder-labs-recalls-grape-multivitamins-due-to-subpotent-vitamin-d.

Source Summary by GovInfoNow · govinfonow.com/recall/7044-winder-labs-recalls-grape-multivitamins-due-to-subpotent-vitamin-d · Updated October 9, 2026 · Official notice: FDA #H-0569-2026

Cite this page

“Winder Labs Recalls Grape Multivitamins Due to Subpotent Vitamin D.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/7044-winder-labs-recalls-grape-multivitamins-due-to-subpotent-vitamin-d. Based on FDA recall #H-0569-2026.

Winder Laboratories, LLC voluntarily recalled Multivitamin with Fluoride Chewable Tablets Grape Flavor after an FDA inspection found the product was subpotent for Vitamin D, according to the Food and Drug Administration on Oct. 27, 2025.

How to tell if you have it

Brand: Winder Laboratories
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
Lot 1692303 SN: 138909557498 EXP: 2025-10-26
Lot 1692304 SN 131163901709 EXP: 2025-10-26
LOT 1712301 SN: 163590222021 EXP: 2025-11-14

The hazard

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

Context

GovInfoNow's records show Winder Laboratories, LLC has two other recalls on record since May 28, 2024. On Nov. 26, 2025, the company recalled Morphine Sulfate Oral Solution due to a mispack size mismatch. On May 28, 2024, Winder Laboratories recalled Phenazopyridine tablets following a product mix-up with phenobarbital.

How to tell if you have this one

Check your bottle for the following details: Product name 'Multivitamin with Fluoride Chewable Tablets Grape Flavor', NDC 75826-169-10 (0.25 mg) or NDC 75826-171-10 (1mg), and UPC codes starting with 3 15826 16910 2 or 3 15826 17110 5. Affected lots are 1692303 (SN: 138909557498), 1692304 (SN: 131163901709), and 1712301 (SN: 163590222021).

Brand
Winder Laboratories
Category
Food

Based on the official FDA remedy

What to do — step by step

Check Your Bottle
Compare your product's lot number, serial number, and NDC against the recalled items listed in the record.
Contact Manufacturer
Since no specific remedy is stated in the record, contact Winder Laboratories directly for further instructions on returns or refunds.

Where it went and when

Where it was distributed

Distributed in 24 states and Puerto Rico.

FDA distribution: “Product was shipped to the following states: 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.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Alabama, Arizona, California, Florida, Hawaii, Illinois, Indiana, Iowa, Massachusetts, Michigan, Mississippi, Missouri, New Jersey, New York, North Carolina, Oregon, Pennsylvania, Puerto Rico, Rhode Island, Tennessee, Texas, Utah, Washington, West Virginia, Wisconsin.

Recall timeline

FDA published this recall 5 months after the firm started it.

Oct 27, 2025Firm started the recall
Mar 13, 2026FDA classified it Class III
Mar 25, 2026Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Link to this recall

<a href="https://govinfonow.com/recall/7044-winder-labs-recalls-grape-multivitamins-due-to-subpotent-vitamin-d">Winder Labs Recalls Grape Multivitamins Due to Subpotent Vitamin D (GovInfoNow)</a>

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #H-0569-2026 (October 27, 2025)
Plain-language summary written by qwen3.6:35b-a3b on October 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.