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Recall Radar/FDA Food Enforcement/F-0462-2021

FDA Food EnforcementMedium / 中

vitafusion Fiber Well 220ct, 10 / 220 CT

Recall F-0462-2021Published 2021-05-05Company Church & Dwight Co., Inc. OGI Distribution Center
Reason / 召回原因Potential presence of a metallic mesh material in products.
Distribution / 销售地区The product was distributed thru out the US and Canada, Panama, China,
Code information / 批次信息Product Code: 027917019840 Lot Codes: WA03087520, WA02487524, WA03086273
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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

F-0462-2021

Classification / 风险等级

Medium / 中

Published / 发布时间

2021-05-05

Recalling firm / 召回企业

Church & Dwight Co., Inc. OGI Distribution Center

Product description / 产品描述

vitafusion Fiber Well 220ct, 10 / 220 CT

Product code / 产品代码

Not provided in the official record

Code information / 批次与代码信息

Product Code: 027917019840 Lot Codes: WA03087520, WA02487524, WA03086273

Product quantity / 产品数量

2928 Bottles

Distribution / 销售地区

The product was distributed thru out the US and Canada, Panama, China,

Reason for recall / 召回原因

Potential presence of a metallic mesh material in products.

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