WHY THIS PRODUCT IS LISTED
Other / see reason
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
Product description & recall reason
The recall record describes “Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.25 mg 100 TABLETS UPC 3 15826 16910 2;…”; the source reports: “Subpotent.”
Based on the official recall record; packaging and sales claims have not been verified. Verify with the official source ↗
Identify the product
- 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
- Brand
- Not supplied by this source
- Lot, batch, UPC & other 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
- Quantity
- 422cs/12/0.25mg/100ct bottles + 210cs/12/1.0mg/100ct bottles
Where it came from & where it went
- Recalling firm
- Winder Laboratories, LLC
- Recalling firm address
- 716 Patrick Industrial Ln; N/A; Winder; GA; 30680-8333; United States
- Product production / origin location
- Not supplied by this source
- Distribution — source wording
- 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.
States identified in the source
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