FDA recall, , Low risk
Winder Laboratories Multivitamin with Fluoride Chewable Tablets
Multivitamin with Fluoride Chewable Tablets are subpotent for Vitamin D.
Summary by Recall Canary from the FDA notice
What happened
Winder Laboratories, LLC of Winder, Georgia, recalled Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx after an FDA inspection discovered the product was subpotent for Vitamin D. The recall began October 27, 2025, and covers the 0.25 mg and 1 mg strengths in 100-tablet bottles.
The product was shipped to Alabama, Arizona, California, Florida, Hawaii, Iowa, Illinois, Indiana, Massachusetts, Michigan, Missouri, Mississippi, North Carolina, New Jersey, New York, Oregon, Pennsylvania, Rhode Island, Tennessee, Texas, Utah, Washington, Wisconsin and West Virginia.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medicine recalls:
- Check the FDA or company notice for instructions specific to this product.
- Ask your pharmacist or doctor whether your lot is affected and what to do.
Is yours affected?
Match the list below, then check the codes the FDA notice also names.
A UPC is the number printed under a barcode. An NDC (National Drug Code) is usually printed on the drug's label.
Multivitamin with Fluoride Chewable Tablets Grape Flavor
- NDC
- 75826-169-10
- 75826-171-10
- UPC
- 3 15826 16910 2
- 3 15826 17110 5
Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx
- Strength
- 0.25 mg
- UPC
- 138909557498
- 131163901709
- 163590222021
- Lot code
- 1692303
- 1692304
- 1712301
From the FDA notice
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
Recall details
- Company began the recall
- Sold in
- 24 states
- Company
- Winder Laboratories, LLCWinder, Georgia
- Hazard
- Wrong drug strength
- Risk
Low risk
Taking it is unlikely to cause health problems.
FDA Class III recall · How risk is rated
- Event ID
- 97884
- Recall number
- H-0569-2026
- Quantity recalled
- 422cs/12/0.25mg/100ct bottles + 210cs/12/1.0mg/100ct bottles
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Listed on Recall Canary
