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Valsartan Recall Lawsuit

The U.S. Food & Drug Administration (FDA) has announced a nationwide recall for valsartan, a widely-prescribed blood pressure medication, after it was found to be contaminated with a substance that has been linked to an increased risk for cancer.

March 9, 2019 – Manufactured by the China-based pharmaceutical company Zhejiang Huahai, Valsartan has been found to contain N-nitrosodimethylamine (NDMA), a chemical health authorities consider a likely human carcinogen (cancer-causing substance), according to a recall announcement the U.S. Food & Drug Administration (FDA).

Free Confidential Lawsuit Evaluation: If you or a loved one has been harmed by the side effects of valsartan, you should contact our law firm immediately. You may be entitled to compensation by filing a suit against the manufacturer and our lawyers can help.

What’s the problem?

The agency originally recalled select lots of Valsartan last month, and has since twice expanded the action to include drugs made by other companies, as well as some tablets with valsartan and hydrochlorothiazide (HCTZ).

Zhejiang Huahai has issued at least 3 major recalls for valsartan products, along with Health Canada and the European Medicines Agency (EMA) conducting their own personal recalls.

In the U.S., FDA has recalled valsartan-containing products from the following companies:

  • A-S Medication Solutions (labeled as Solco Healthcare)
  • Bryant Ranch Prepack
  • HJ Harkins Company
  • Northwind Pharmaceuticals
  • Prinston Pharmaceutical Inc. (labeled as Solco Healthcare)
  • Teva Pharmaceuticals Industries Ltd. (some labeled as Actavis, some as Major Pharmaceuticals)
  • AvKARE
  • A-S Medication Solutions
  • Northwind Pharmaceuticals
  • Prinston Pharmaceutical (labeled as Solco Healthcare)
  • Proficient Rx
  • Remedy Repack
  • Teva Pharmaceuticals (some labeled as ACtavis)

FDA advises consumers who are taking a medication with valsartan to compare their prescription bottle to the agency’s list to determine whether their drugs have been recalled. Patients can also contact their pharmacist, who may be able to provide valsartan from a pharmaceutical company not involved in the recall.

Patients taking these medications should continue using them until their doctor or pharmacist has a replacement drug or treatment, FDA says.

What is NDMA?

All of the valsartan recalls were issued over concerns of potential contamination with N-nitrosodimethylamine (NDMA), according to the U.S. Environmental Protection Agency (EPA). NDMA is a semivolatile organic chemical that belongs to the N-ni-trosamines family of potent carcinogens. The chemical is not currently produced in pure form or commercially used in the U.S., except for research purposes. It was formerly used in production of liquid rocket fuel, antioxidants, additives for lubricants and softeners for copolymers, according to the EPA.

Do I Have a Valsartan Lawsuit?

The Pharmaceutical Litigation Group at our law firm is an experienced team of trial lawyers that focus on the representation of plaintiffs in valsartan lawsuits. We are handling individual litigation nationwide and currently accepting new valsartan side effects cases in all 50 states.

Free Confidential Lawsuit Evaluation: Again, if you or a loved one got cancer after taking valsartan, you should contact our law firm immediately. You may be entitled to a settlement by filing a suit and we can help.

Free Confidential Case Evaluation

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