intraKID Lot 658 with a Best By date of 12/12 — Class II food recall F-2126-2012
Terminated recall by Drucker Labs LP, reported 2012-09-12, distributed nationwide. After extensive testing and investigation, Drucker Labs has determined that an incorrect form of Vitamin B3, N
| Recall number | F-2126-2012 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Drucker Labs LP, Plano, TX, United States |
| Recall initiated | 2012-08-13 |
| Classified | 2012-09-05 |
| Reported by FDA | 2012-09-12 |
| Terminated | 2014-10-07 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 2,026 bottles |
| Lot numbers | 658 |
Product
intraKID Lot 658 with a Best By date of 12/12, 33 oz and 2 oz bottles
Reason for recall
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-2126-2012. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.