intraKID Lot 658 with a Best By date of 12/12 recall
Recalled by Drucker Labs LP · Plano, TX, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
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
See the recall's own reason text for the specifics. All other reasons recalls.
What was recalled
intraKID Lot 658 with a Best By date of 12/12, 33 oz and 2 oz bottles
Quantity: 2026 bottles
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot 658 with a Best By date of 12/12
Where it was sold
Nationwide.
FDA's distribution note: Nationwide and to Canada
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Drucker Labs LP
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Aug 13, 2012
- In FDA report of
- Sep 12, 2012
- Terminated
- Oct 7, 2014
- FDA recall number
- F-2126-2012 · event 62872
- Official record
- FDA enforcement report search