Zantac Pill

Zantac Cancer Risks and Recalls

Millions of Americans have taken Zantac or its generic form, ranitidine, for acid reflux or GERD each year since the 1980s. In April 2020, manufacturers withdrew the popular heartburn drug from the U.S. market because of a potential cancer-causing contaminant called NDMA. Drugwatch’s guide explains how ranitidine products could expose users to unacceptable risks and tells you how to take legal action if you developed cancer after taking Zantac.

Find Out If You Qualify for Compensation

If you or a loved one took Zantac and were diagnosed with cancer, you may be eligible for compensation. In this guide, you’ll learn which cancers are included in lawsuits and what questions a Zantac lawyer may ask.

Take A Look Inside

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    Zantac Recalls
  • Icon - NDMA
    How Dangerous is NDMA in Zantac?
  • Icon - IV
    Cancer Lawsuits
  • Icon - Gavel
    Am I Eligible to File a Lawsuit?
  • Icon - Lawyer
    Questions a Lawyer May Ask
  • Icon - Checklist
    Patient Checklist
Please seek the advice of a medical professional before making health care decisions.