FDA · Drugs ·
Primidone Tablets recall
Amerisource Health Services LLC recalled Primidone Tablets on May 27, 2026 because of cross contamination with other products: API contaminated with trace amounts of Acemetacin API. It was sold nationwide.
Why it was recalled
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
What's recalled
Primidone Tablets, USP, 250 mg, 100 Tablets (10 x 10 unit dose blister) per carton, Rx only, Distributed by: American Health Packaging, Columbus, Ohio 43217. Carton NDC: 68084-203-01; Individual Dose NDC: 68084-203-11
Quantity: 63,500 tablets
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- Amerisource Health Services LLC, Columbus, OH
- Date
- Severity
- Class III
the product is unlikely to cause health problems but breaks a rule. - Where sold
- Nationwide
USA Nationwide - Status
- Ongoing
- Recall number
- D-0536-2026
- Source
- U.S. Food and Drug Administration
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