Class IIIOngoingVoluntary: Firm initiated
Winder Laboratories, LLC: food recall H-0569-2026
Winder Laboratories, LLC of Winder, GA recalled Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.25 mg 100 TABLETS UPC 3 15826 16910 2;… Reason: Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D. The FDA listed it as Class III in its Enforcement Report dated Mar 25, 2026; distribution: Alabama, Arizona, California, Florida, Hawaii, Iowa, Illinois, Indiana, Massachusetts, Michigan, Missouri, Mississippi, North Carolina, New Jersey, New York, Oregon, Pennsylvania, Puerto Rico, Rhode Island, Tennessee, Texas, Utah, Washington, Wisconsin, West Virginia.
Record status as published: Ongoing. openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- 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
- Product quantity
- 422cs/12/0.25mg/100ct bottles + 210cs/12/1.0mg/100ct bottles
- Reason for recall
- Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
- Codes, lots and dates on the package
- Lot 1692303 SN: 138909557498 EXP: 2025-10-26 & Lot 1692304 SN 131163901709 EXP: 2025-10-26; LOT 1712301 SN: 163590222021 EXP: 2025-11-14
- Distribution pattern
- 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.
- Recalling firm
- Winder Laboratories, LLC, Winder, GA
- Classification
- Class III — the FDA uses this class for a situation in which using or being exposed to the product is not likely to cause adverse health consequences.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Letter
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Oct 27, 2025 |
| Classified by the FDA | Mar 13, 2026 |
| Published in the Enforcement Report | Mar 25, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0569-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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