Primidone Tablets 50 mg
Primidone 50 mg tablets recalled due to possible cross-contamination with Acemetacin.
Stop using the recalled Primidone Tablets and contact your healthcare provider for guidance. Return the product to the place of purchase for a refund or replacement.
Why it was recalled
Golden State Medical Supply is recalling Primidone Tablets, USP, 50 mg, 50-count bottles, because the active ingredient may be cross-contaminated with trace amounts of Acemetacin, a different drug. This contamination could cause unexpected side effects or interactions in patients taking the medication.
Is mine affected?
Check the NDC or UPC and strength printed on the package. Yours is affected if it matches one below.
Primidone Tablets, USP
| Lot code | Strength | NDC / UPC | Recall # |
|---|---|---|---|
| GS067909, 2028 | 250 mg | NDC 51407-638-01 | D-0535-2026 |
| GS066750, GS067084, GS067710, GS067873, 2028 | 50 mg | NDC 51407-637-05 | D-0534-2026 |
Where it was sold
Distributed nationwide.
Timeline
- Firm initiated recall
- Publicly announced
- Listed on Recall Canary
- Summary updated
Official source
Other recent recalls from Golden State Medical Supply Inc.
Editorial summary by Recall Canary · summary updated 2026-09-08 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification