Drucker Labs, LP
FEI 3008204695 · 1600 Capital Ave Ste 100, Plano, Texas, 75074, United States
1 warning letter on record
Per FDA, as of 2026-10-31 · Sources: FDA Data Dashboard, Import Alerts, Enforcement Reports
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Import alerts
0
Import refusals (5 years)
0
Warning letters
1
Last FDA action
2026-08-21
2 months ago
FDA record
- 2012-08-13RecallRecall F-2126-2012 · Class 2 · 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 minutintraKID Lot 658 with a Best By date of 12/12, 33 oz and 2 oz bottlesSource: FDA Enforcement Reports