Class III
Drug Recall: Primidone Tablets, USP, 250 mg, 100-count bottle, RX only, Manufactured by: Lannett Company, Inc., Marketed by: GSMS, Incorporated, Camarillo, CA 93012. NDC 51407-638-01
Golden State Medical Supply Inc. · April 27, 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
1,620 bottles
Source: FDA (openFDA Drug Enforcement)
Recall number: D-0535-2026
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.