Recalls / Class II

Class IID-0981-2018

Product

Valsartan and Hydrochlorothiazide (HCTZ) Tablets, USP 80 mg/12.5 mg tablets, 90 count-count bottle, Rx Only, Manufactured by: Arrow Pharma (Malta) Ltd. India, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054, NDC 0591-2315-19.

Affected lot / code info

Lot # 1191191M, 1191192M, 1191193M, 1191194M, 1191195M, 1238466M, 1238467M, 1253261M 1256125M, 1277709M

Why it was recalled

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

Recalling firm

Firm

Teva Pharmaceuticals USA

Notification channel

Press Release

Type

Voluntary: Firm initiated

Address

1090 Horsham Rd, N/A, North Wales, Pennsylvania 19454-1505

Distribution

Quantity

56,603 bottles

Distribution pattern

Product was distributed throughout the United States, including Hawaii and Puerto Rico

Timeline

Recall initiated

2018-07-16

FDA classified

2018-07-24

Posted by FDA

2018-08-01

Status

Ongoing

Source: openFDA Drug Enforcement endpoint. Recall record D-0981-2018. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.