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.