Drucker Labs LP: Food Recall in 2012 - (Recall #: F-2126-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: August 13, 2012

Date Posted: September 12, 2012

Recall Number: F-2126-2012

Event ID: 62872

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

Status: Terminated

Product Quantity: 2026 bottles

Code Information:

Lot 658 with a Best By date of 12/12

Distribution Pattern:

Nationwide and to Canada

Voluntary or Mandated:

Voluntary: Firm initiated