intraKID Lot 658 with a Best By date of 12/12
Recalling firm: Drucker Labs LP
Why it was 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
The exact product
intraKID Lot 658 with a Best By date of 12/12, 33 oz and 2 oz bottles
Check the codes
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Original FDA code information
Lot 658 with a Best By date of 12/12
Recall details
- Recall number
- F-2126-2012
- Event ID
- 62872
- FDA status
- Terminated
- Initiated
- Aug 13, 2012
- Reported
- Sep 12, 2012
- Classified
- Sep 5, 2012
- Terminated
- Oct 7, 2014
- Quantity
- 2026 bottles
- Location
- Plano, TX, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Letter
Where it was distributed
Nationwide and to Canada
Data updated September 16, 2026. View official FDA data ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.