FDA Food recall ·
Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx recall
- Recall number
- H-0569-2026
- Date
- (initiated October 27, 2025)
- Company / brand
- Winder Laboratories, LLC
716 Patrick Industrial Ln, Winder, GA, United States - Category
- Food › Class III
- Classification
- Class III
- Status
- Ongoing
- Units affected
- 422cs/12/0.25mg/100ct bottles + 210cs/12/1.0mg/100ct bottles
- Hazard tags
- Potency
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
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
Why was it recalled?
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot 1692303 SN: 138909557498 EXP: 2025-10-26 & Lot 1692304 SN 131163901709 EXP: 2025-10-26; LOT 1712301 SN: 163590222021 EXP: 2025-11-14
Distribution
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: 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
What does Class III mean?
Class III means use of or exposure to the product is not likely to cause adverse health consequences (for example, a labeling violation).
Source: FDA (food), recall H-0569-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.