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Recall Radar/FDA Food Enforcement/F-2126-2012

FDA Food EnforcementMedium / 中

intraKID Lot 658 with a Best By date of 12/12, 33 oz and 2 oz bottles

Recall F-2126-2012Published 2012-09-12Company Drucker Labs LP
Reason / 召回原因After extensive testing and investigation, Drucker Labs has determined that an incorrect form of Vitamin B3, Nicotinic Acid, was used in the manufacturing of intraKID Lot 658. This nutrient may cause a temporary symptom in a small number of consumers. This symptom, commonly known as Niacin Flush, may include itching, redness, or warmth of the skin. This typically subsides within 15  20 minut
Distribution / 销售地区Nationwide and to Canada
Code information / 批次信息Lot 658 with a Best By date of 12/12
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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-2126-2012

Classification / 风险等级

Medium / 中

Published / 发布时间

2012-09-12

Recalling firm / 召回企业

Drucker Labs LP

Product description / 产品描述

intraKID Lot 658 with a Best By date of 12/12, 33 oz and 2 oz bottles

Product code / 产品代码

Not provided in the official record

Code information / 批次与代码信息

Lot 658 with a Best By date of 12/12

Product quantity / 产品数量

2026 bottles

Distribution / 销售地区

Nationwide and to Canada

Reason for recall / 召回原因

After extensive testing and investigation, Drucker Labs has determined that an incorrect form of Vitamin B3, Nicotinic Acid, was used in the manufacturing of intraKID Lot 658. This nutrient may cause a temporary symptom in a small number of consumers. This symptom, commonly known as Niacin Flush, may include itching, redness, or warmth of the skin. This typically subsides within 15  20 minut

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