MODERATE RISK Terminated F-2126-2012

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

Recalled by Drucker Labs LP

Classification

Class II — Products that might cause a temporary health problem, or pose only a slight threat of a serious nature.

Reason for Recall

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

Product Details

Product Quantity
2026 bottles
Product Type
Food
Code Info
Lot 658 with a Best By date of 12/12
Voluntary/Mandated
Voluntary: Firm initiated

Distribution & Geography

Distribution Pattern
Nationwide and to Canada
Company Location
Plano, TX, 75074-8187

Timeline

Report Date
09/12/2012
Recall Initiated
08/13/2012
Classification Date
09/05/2012
Termination Date
10/07/2014

Source: U.S. Food & Drug Administration (FDA) — FDA Recalls

Last updated: August 29, 2026

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