FDA Food EnforcementOther / 其他

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
Reason / 召回原因Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
Distribution / 销售地区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.
Code information / 批次信息Lot 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 / 官方信息说明
This page organizes fields from the named agency record. It is not medical, legal, or food-safety advice. Always compare your package with the official notice.

Official record details

官方记录详情:以原始机构公告为准

Recall number / 召回编号

H-0569-2026

Classification / 风险等级

Other / 其他

Published / 发布时间

2026-03-25

Recalling firm / 召回企业

Winder Laboratories, LLC

Product description / 产品描述

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 / 产品代码

Not provided in the official record

Code information / 批次与代码信息

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 / 产品数量

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

Distribution / 销售地区

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 / 召回原因

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

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Last synchronized: 2026-08-09. Recall Radar does not replace agency guidance.