FDA recall record
intraKID Lot 658 with a Best By date of 12/12, 33 oz and 2 oz bottles
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of October 7, 2014. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
intraKID Lot 658 with a Best By date of 12/12, 33 oz and 2 oz bottles
Reason
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
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
intraKID Lot 658 with a Best By date of 12/12, 33 oz and 2 oz bottles
Code information listed by FDA
Lot 658 with a Best By date of 12/12
Distribution and firm information
Recalling firm listed by FDA: Drucker Labs LP
Firm location listed by FDA: Plano, TX, United States
Distribution reported by FDA: Nationwide and to Canada
Product quantity listed by FDA: 2026 bottles
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.