RecallRadar

FDA Drug recall D-0534-2026

Primidone Tablets, USP, 50 mg, 50-count bottle, RX only, Manufactured by: Lannett Company, Inc., Marketed by: GSMS, Incorporated, Camarillo…

On 2026-05-27 the FDA classified a Class III recall of Primidone Tablets, USP, 50 mg, 50-count bottle, RX only, Manufactured by: Lannett Company, Inc., Marketed by: GSMS, Incorporated, Camarillo… by Golden State Medical Supply, citing cross contamination with other products: API contaminated with trace amounts of Acemetacin API.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0534-2026
ClassificationClass III
Statusongoing
Initiated2026-04-27
Published2026-05-27
Last updated2026-09-13 11:52 UTC
CompanyGolden State Medical Supply
DistributionUS

Product

Primidone Tablets, USP, 50 mg, 50-count bottle, RX only, Manufactured by: Lannett Company, Inc., Marketed by: GSMS, Incorporated, Camarillo, CA 93012. NDC 51407-637-05

Reason

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

Identifiers

ndc51407-637-01
ndc51407-637-05
ndc51407-638-01
code_infoLot#: GS066750, GS067084, GS067710, GS067873, Exp 3/31/2028; GS068339, GS068897, Exp 8/31/2028

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0534-2026%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.