F-2126-2012 Class II Terminated

Recalled by Drucker Labs LP — Plano, TX

Recall Details

Product Type
Food
Report Date
September 12, 2012
Initiation Date
August 13, 2012
Termination Date
October 7, 2014
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
2026 bottles

Product Description

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

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

Distribution Pattern

Nationwide and to Canada

Code Information

Lot 658 with a Best By date of 12/12