FDA Food EnforcementOther

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

Recall H-0569-2026Published 2026-03-25Company Winder Laboratories, LLC
ReasonSubpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
DistributionProduct 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.
Code informationLot 1692303 SN: 138909557498 EXP: 2025-10-26 & Lot 1692304 SN 131163901709 EXP: 2025-10-26; LOT 1712301 SN: 163590222021 EXP: 2025-11-14
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Official-information notice
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Official record details

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Recall number

H-0569-2026

Classification

Other

Published

2026-03-25

Recalling firm

Winder Laboratories, LLC

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

Product code

This field was not provided in the official notice. Please confirm in the original notice.

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

Product quantity

422cs/12/0.25mg/100ct bottles + 210cs/12/1.0mg/100ct bottles

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.

Reason for recall

Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.

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Editorial review: Foods Recall Editorial Team
Last synchronized: 2026-09-20. Foods Recall does not replace agency guidance.