US Drug Recall Register
Class II · Moderate risk Terminated Initiated Nov 29, 2017 (9 years ago)

Valsartan Tablets, USP, 160 mg, 90-count bottles, Rx Only, Manufactured by: Zhejiang…

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

Why it was recalled

Failed Tablet/Capsule Specifications: confirmed customer complaint of thicker and heavier tablets in bottle.

What was recalled

Valsartan Tablets, USP, 160 mg, 90-count bottles, Rx Only, Manufactured by: Zhejiang Huahai Pharmaceutical Co., Ltd, Xunqiao, Linhai, Zhejiang 317024, China; Distributed by: Solco Healthcare US, LLC, Cranbury, NJ 08512, USA; NDC 43547-369-09.

Recalling firm
Prinston Pharmaceutical Inc
NDC code
43547-369-09
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0209-2018

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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