Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

intraKID Lot 658 with a Best By date of 12/12 Recalled by Drucker Labs LP Due to After extensive testing and investigation, Drucker Labs has...

Date: August 13, 2012
Company: Drucker Labs LP
Status: Terminated
Source: FDA (Food)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Drucker Labs LP directly.

Affected Products

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

Quantity: 2026 bottles

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Drucker Labs LP

Drucker Labs LP has 1 total recall tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Food). Last updated March 26, 2026. View original report