Reported Aug 1, 2018 · Ongoing
Valsartan Tablets, USP 320 mg, 90-count bottle (NDC 0591-2170-19), 500-count bottle (NDC 0591-2170-05), Rx Only, Rx…
Teva Pharmaceuticals USA
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Teva Pharmaceuticals USA · 1090 Horsham Rd · North Wales, PA · 19454-1505
Is this the product you have?
- Valsartan Tablets, USP 320 mg, 90-count bottle (NDC 0591-2170-19), 500-count bottle (NDC 0591-2170-05), Rx Only, Rx Only
- Manufactured byArrow Pharma (Malta) Ltd. India
- Distributed byActavis Pharma, Inc. Parsippany, NJ 07054
- Lot codes and dates
- NDC 0591-2170-19 Lot Numbers
1208002A1247282M1263944M
- NDC 0591-2170-05 Lot Numbers
1208000M1208001M1240425A
- NDC 0591-2170-19 Lot Numbers
- Amount recalled
- 13,555 90-count bottles; 2,892 500-count bottles
This recall covers 9 products
The agency filed one notice per product. You are reading one of them; the other 8 are below.
Where it was sold
Why it was recalled
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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