Skip to main content
Recall Canary
Primidone Tablets 50 mg
← Back to all recalls
DRUG RECALLLOW

Primidone Tablets 50 mg

Golden State Medical Supply is recalling Primidone Tablets 50 mg due to cross-contamination with trace amounts of Acemetacin API.

What to do

Stop using the affected medication and contact your healthcare provider or pharmacist for further guidance.

Posted
Updated
Recall No.
D-0535-2026
Agency
Firm
Golden State Medical Supply Inc.
Recall ID
98856
Status
ONGOING

Why it was recalled

Golden State Medical Supply is recalling Primidone Tablets, USP, 50 mg, 50-count bottles due to cross-contamination with trace amounts of Acemetacin API. The product was distributed nationwide.

Is mine affected?

Check the NDC or UPC and strength printed on the package. Yours is affected if it matches one below.

ProductRecall #
Primidone Tablets, USP, 250 mg, 100-count bottle, RX only, Manufactured by: Lannett Company, Inc., Marketed by: GSMS, Incorporated, Camarillo, CA 93012. NDC 51407-638-01D-0535-2026
Primidone Tablets, USP, 50 mg, 50-count bottle, RX only, Manufactured by: Lannett Company, Inc., Marketed by: GSMS, Incorporated, Camarillo, CA 93012. NDC 51407-637-05D-0534-2026

Where it was sold

Distributed nationwide.

Other recent recalls from Golden State Medical Supply Inc.

← Back to all recalls

Editorial summary by Recall Canary · last updated 2026-07-13 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification