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FDAFDA · Food and drugs·Recall number D-0983-2018

Valsartan and Hydrochlorothiazide (HCTZ) Tablets, USP 160 mg/25 mg tablets, USP 90-count bottle, Rx Only, Rx Only, Manufactured by: Arrow Pharma (Malta) Ltd. India, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054. NDC 0591-2317-19.

Published August 1, 2018 · Recall initiated: July 16, 2018

Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

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

What to do

Voluntary: Firm initiated · Press Release

Recall details

Manufacturer
Teva Pharmaceuticals USA
Distributor
Product was distributed throughout the United States, including Hawaii and Puerto Rico
Lot
Lot Numbers: 1191164M, 1191165M, 1191166M, 1191167A, 1225612M, 1250717M, 1256111M, 1288798M
Risk classification
Class II
Area (FDA)
drug
Country
United States

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