Nationwide Representation - Heartburn Medication Contaminated with Cancer-Causing NDMA
Zantac (ranitidine) was recalled worldwide after it was discovered that the popular heartburn medication contained NDMA, a probable human carcinogen. Millions of people who took Zantac may have been exposed to dangerous levels of this cancer-causing substance.
Zantac contained N-Nitrosodimethylamine (NDMA), a probable human carcinogen that can cause cancer.
Zantac was one of the most popular over-the-counter and prescription heartburn medications for decades.
The FDA and health authorities worldwide recalled Zantac products due to NDMA contamination concerns.
You regularly took Zantac (ranitidine) for heartburn, acid reflux, or other stomach conditions.
You were diagnosed with stomach, bladder, liver, kidney, or other cancers linked to NDMA exposure.
You used Zantac for an extended period, increasing your exposure to NDMA contamination.
Your cancer diagnosis occurred after taking Zantac products containing NDMA.
You may be entitled to compensation for medical expenses, pain and suffering, and lost wages. Get your free case review today.