FDA recalls · F-2126-2012
Drucker Labs LP recall
- FoodintraKID Lot 658 with a Best By date of 12/12, 33 oz and 2 oz bottles
- ReasonAfter 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
- ClassClass II: the food could cause temporary or treatable health problems
- StatusClosed by FDA, ended 2014-10-07
- DatesFirm started it 2012-08-13. In FDA's enforcement report 2012-09-12.
- Sold inNationwide and to Canada
- Amount2026 bottles
- CodesLot 658 with a Best By date of 12/12
- FirmDrucker Labs LP, Plano, TX · Voluntary: Firm initiated
Products we list
None. We tie a recall to a product only by a barcode printed in the recall, and this one names none we list. That does not mean the recalled food is missing from our listings.
From FDA's enforcement report, via openFDA (CC0): raw data for this recall. FDA's own Enforcement Report search finds it by its number, F-2126-2012. Class meanings: FDA.