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FSFood Safety Notice
FDA source record

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

Readable source details for FDA recall record H-0569-2026.

FDA recall number
H-0569-2026
FDA event ID
97884
Company
Winder Laboratories, LLC
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
Reason for recall
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
Classification
Class III
Status
Ongoing
Recall date
Mar. 25, 2026
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.

Technical source

This page reformats the FDA enforcement record for readability. The original machine-readable record is available for verification.

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