US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jul 18, 2018 (8 years ago)

Unit Dose Valsartan Tablets, USP. 160 mg. Rx only.,Distributed by: Major…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.

What was recalled

Unit Dose Valsartan Tablets, USP. 160 mg. Rx only.,Distributed by: Major Pharmaceuticals, Livonia, MI 48152, NDC# 0904-6594-61. NDC# 0904-6595-61.

Recalling firm
Major Pharmaceuticals
NDC code
0904-6594-61
Origin
MI, United States
Initiated by
N/A
FDA recall number
D-0967-2018

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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