FreshRecalls

⚠ Data freshness notice: the most recent refresh of NHTSA was incomplete, so a very recent recall may be missing. Everything shown is accurate as of the last checked time on this page — for anything time-critical, confirm with the official sources linked below.

FDAClass III · Drug · Recalled May 27, 2026

Primidone Tablets recall — Golden State Medical Supply Inc.

Hazard: Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.

Class III: not likely to cause adverse health consequences.

View the official FDA enforcement record (openFDA) ↗

Official recall ID
D-0535-2026
Brand
Golden State Medical Supply
Classification
Class III
Units affected
1,620 bottles
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Description

Primidone Tablets, USP, 250 mg, 100-count bottle, RX only, Manufactured by: Lannett Company, Inc., Marketed by: GSMS, Incorporated, Camarillo, CA 93012. NDC 51407-638-01

Affected products

Companies & origin

Recalling firm location
Camarillo, CA, United States
Firm address
5187 Camino Ruiz, 93012-8601

Identifying details (verbatim from the notice)

Product codes / lots
Lot #: GS067909, Exp 4/30/2028; GS068646, Exp 8/31/2026
Distribution
USA Nationwide
Firm notified the public via
Letter
FDA event ID
98856
Recall initiated
April 27, 2026
FDA classified
May 18, 2026
FDA report date
May 27, 2026

Source: U.S. Food & Drug Administration. This page mirrors the official public-domain record verbatim; the linked government source is authoritative. Source last checked July 23, 2026 at 11:04 PM UTC.

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