FDAFDA · Food and drugs·Recall number F-2126-2012
intraKID Lot 658 with a Best By date of 12/12, 33 oz and 2 oz bottles
Published September 12, 2012 · Recall initiated: August 13, 2012
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Drucker Labs LP
- Distributor
- Nationwide and to Canada
- Lot
- Lot 658 with a Best By date of 12/12
- Risk classification
- Class II
- Area (FDA)
- food
- Country
- United States
Sell products like this?
Recalert watches your whole catalog for recalls like this one, automatically.