Home / Food recalls / 2012
Drucker Labs LP
FDA recall F-2126-2012 · Class II · reported 2012-09-12 · Terminated
- Product
- intraKID Lot 658 with a Best By date of 12/12, 33 oz and 2 oz bottles
- Reason
- 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
- Quantity
- 2026 bottles
- Distribution
- Nationwide and to Canada
- Firm location
- TX, United States
- Initiated
- Voluntary: Firm initiated
- First notice
- Letter
- Recall started
- 2012-08-13
- Terminated
- 2014-10-07
- Code info
- Lot 658 with a Best By date of 12/12
Source: U.S. Food and Drug Administration, openFDA Food Enforcement database (openFDA Food Enforcement, imported 2026-09). The FDA does not validate openFDA data for completeness or accuracy. This is a record of an enforcement action, not safety advice.