US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jul 26, 2018 (8 years ago)

Valsartan tablets 160 mg, 90-count bottle, Rx Only, Repackaged by H.J. Harkins Co, Inc…

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

Why it was recalled

Carcinogen impurity detected in API used to manufacture drug product.

What was recalled

Valsartan tablets 160 mg, 90-count bottle, Rx Only, Repackaged by H.J. Harkins Co, Inc. Grover Beach, CA 93433, NDC 43547-0369-09. Tablet is yellow, capsule-shaped, biconvex, film-coated tablets debossed with 343 on one side and HH on the other side.

Recalling firm
H J Harkins Company Inc dba Pharma Pac
NDC code
43547-0369-09
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1022-2018

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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