Class III

Drug Recall: Primidone Tablets USP, 250mg, 100-count bottle, Rx only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136, NDC 0527-1231-01.

Lannett Company Inc. · April 24, 2026

Reason for Recall

Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.

Distribution

USA Nationwide

States Affected

NATIONWIDE

Quantity Affected

44865 bottles

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0533-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.