• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Enforcement Report - Week of September 12, 2012

  • Print
  • Share
  • E-mail

Product Detail

Product Description intraKID Lot 658 with a Best By date of 12/12, 33 oz and 2 oz bottles
Recall Number F-2126-2012
Classification Class II
Code Info Lot 658 with a Best By date of 12/12
Product Distributed Qty 2026 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 minutes and has no long-term side effects.

Event Detail

Event Id 62872
Product Type Food
Status Ongoing
Recalling Firm Drucker Labs LP
City Plano
State TX
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2012-08-13
Initial Firm Notification of Consignee or Public Letter
Distribution Pattern Nationwide and to Canada