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
Reason for recall
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
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- Event ID
- 97884
- Code info
- Lot 1692303 SN: 138909557498 EXP: 2025-10-26 & Lot 1692304 SN 131163901709 EXP: 2025-10-26; LOT 1712301 SN: 163590222021 EXP: 2025-11-14
- Product quantity
- 422cs/12/0.25mg/100ct bottles + 210cs/12/1.0mg/100ct bottles
- 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.
- Voluntary / mandated
- Voluntary: Firm initiated
- Initial firm notification
- Letter
- Product type
- Food
- Recalling firm location
- 716 Patrick Industrial Ln, N/A, Winder, GA, United States
- Recall initiation date
- 10/27/2025
- Center classification date
- 03/13/2026