Golden State Medical Supply recalls Primidone Tablets (250mg) due to cross contamination with Acemetacin. Affected lots may pose health risks. Consumers should contact the manufacturer for details.
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
Golden State Medical Supply is recalling Primidone Tablets (250mg, 100-count) because they may contain trace amounts of Acemetacin from cross contamination. This could pose health risks to patients using the medication.
The tablets may have been contaminated with trace amounts of Acemetacin during manufacturing. This cross contamination could lead to unintended medication effects if taken by patients.
Patients prescribed Primidone Tablets by a doctor are affected. Those using the recalled lot numbers are most at risk.
Check for the lot numbers GS067909 (expiring 4/30/2028) or GS068646 (expiring 8/31/2026) on the bottle. The product is a 250mg Primidone Tablets, USP, 100-count bottle, prescription-only item.
Look for the lot numbers GS067909 (expiring 4/30/2028) or GS068646 (expiring 8/31/2026) on the bottle.
The tablets may contain trace amounts of Acemetacin due to cross contamination during manufacturing.
The official recall notice does not specify a remedy or action steps for affected consumers.
Check for the lot numbers GS067909 (expiring 4/30/2028) or GS068646 (expiring 8/31/2026) on the bottle.
We’ve drafted a message you can send Golden State Medical Supply to request your refund or repair — edit it as you like.
Subject: Recall D-0535-2026 — Golden State Medical Supply Golden State Medical Supply Hello, I own a Golden State Medical Supply that is covered by recall D-0535-2026 from Golden State Medical Supply. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.