US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jul 27, 2018 (8 years ago)

Valsartan 320 mg tablets, 90-count bottles ( NDC 71335-0567-2), Rx Only, Packaged by…

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

Valsartan 320 mg tablets, 90-count bottles ( NDC 71335-0567-2), Rx Only, Packaged by Bryant Ranch, Burbank, CA 91504.

Recalling firm
Bryant Ranch Prepack Inc.
NDC code
71335-0567-2
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1029-2018

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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