Recall

Low health risk

Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.25 mg 100…

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

FDA recall notices

This row is from FDA’s lot file, which does not include a public page per product. The button opens FDA’s published recall list.

What to do

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  1. 1Compare your product and package codes with the affected products below.
  2. 2If they match, do not eat or serve the product.
  3. 3Follow the official notice for return or disposal instructions.

Recall details

Firm
Winder Laboratories, LLC
Status
Ongoing
Reported
Mar 25, 2026
Started
Oct 27, 2025
Where sold
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.
Quantity
422cs/12/0.25mg/100ct bottles + 210cs/12/1.0mg/100ct bottles

Lots, UPC, dates

Lot 1692303 SN: 138909557498 EXP: 2025-10-26 & Lot 1692304 SN 131163901709 EXP: 2025-10-26; LOT 1712301 SN: 163590222021 EXP: 2025-11-14

Agency wording

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

Source: FDA report. This is not medical advice. Compare your package codes before you act.