F-2126-2012 Class II Terminated
FDA food recall F-2126-2012 was initiated by Drucker Labs LP on August 13, 2012 and is designated Class II. 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… The recall status is terminated (terminated October 7, 2014). Affected quantity: 2026 bottles.
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