FDAFDA · Food and drugs·Recall number D-0534-2026
Primidone Tablets, USP, 50 mg, 50-count bottle, RX only, Manufactured by: Lannett Company, Inc., Marketed by: GSMS, Incorporated, Camarillo, CA 93012. NDC 51407-637-05
Published May 27, 2026 · Recall initiated: April 27, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- PRIMIDONE
- Manufacturer
- Golden State Medical Supply Inc.
- Distributor
- USA Nationwide
- Lot
- Lot#: GS066750, GS067084, GS067710, GS067873, Exp 3/31/2028; GS068339, GS068897, Exp 8/31/2028
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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