Why it was recalled
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
Product description
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
Lot numbers, UPCs & expiration 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
Where it was 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.
What to do if you have this product
- Compare the brand, size, and lot/UPC codes on your package with the codes above.
- If it matches, don't eat it. Return it to the store for a refund or throw it away.
- Wash surfaces and containers that touched the product.
- If you feel sick after eating it, contact your doctor. In an emergency call 911.
Recall details
- Recall number
- H-0569-2026
- Classification
- Class III
- Status
- Ongoing
- Recall initiated
- Oct 27, 2025
- FDA report date
- Mar 25, 2026
- Quantity
- 422cs/12/0.25mg/100ct bottles + 210cs/12/1.0mg/100ct bottles
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Winder Laboratories, LLC
Original FDA data
Every field from FDA enforcement report H-0569-2026, exactly as published.
Show all FDA fields
- City
- Winder
- State
- GA
- Status
- Ongoing
- Country
- United States
- Event ID
- 97884
- Address
- 716 Patrick Industrial Ln
- Code information
- Lot 1692303 SN: 138909557498 EXP: 2025-10-26 & Lot 1692304 SN 131163901709 EXP: 2025-10-26; LOT 1712301 SN: 163590222021 EXP: 2025-11-14
- Postal code
- 30680-8333
- Report date
- Mar 25, 2026
- Product type
- Food
- Recall number
- H-0569-2026
- Classification
- Class III
- Recalling firm
- Winder Laboratories, LLC
- 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.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- 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
- 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.
- Recall initiation date
- Oct 27, 2025
- Initial firm notification
- Letter
- Center classification date
- Mar 13, 2026