Year: 2020

Zantac pills spilled out of the bottle.

The U.S. Food and Drug Administration has pulled the popular heartburn medication Zantac (generic ranitidine) off store shelves after testing revealed dangerous levels of N-Nitrosodimethlyamine (NDMA) in some of its samples. NDMA is classified as a probable human carcinogen, or a substance that could cause cancer. The recall includes both…