Zantac Cancer Lawsuit

See If You Qualify For Compensation

Time Is Limited

You may be entitled to significant compensation

The FDA issued a recall on Zantac due to high levels of NDMA (Nitrosodimethylamine)

NDMA has been declared a probable human carcinogen by the World Health Organization and the Environmental Protection Agency

If you've used Zantac and suffered from any of these cancers you may be qualified for compensation

  • Bladder Cancer
  • Brain Cancer
  • Colorectal Cancer
  • Esophogeal Cancer
  • Kidney (Renal) Cancer
  • Liver Cancer
  • Pancreatic Cancer
  • Prostate Cancer

FDA Issues Recall

Due to high levels of NDMA, the FDA determined that the heatburn drug Zantac posed a risk to public health. NDMA is not only an ingredient in rocket fuel, it is used in lab tests to afflict animals with cancer. NDMA is classified as a probable carcinogen by the WHO and the EPA.

The FDA recommends no more than 96 nanograms of NDMA daily, but tests show a tablet of Zantac contains more than 3 million nanograms. Zantac has long known about the presence of NDMA in their product, yet they failed to alert consumers, doctors or regulators about its presence.They chose profitability over the safety of consumers. may have to contact you occasionally to help you with your evaluation. By pressing the submit button below, you give SSDI Network your consent to use automated technology to call you at the phone number(s) listed above, including your wireless number if provided. Please note that you are not required to provide this consent to utilize our services. By entering my information and clicking “SUBMIT” I am providing express consent to be contacted by via email, phone and text, including my wireless phone number, regarding product and servicing information using automated technology. Standard message and data rates may apply to text messages. I also understand that I may be contacted by and its affiliates via email and/or phone