FDA issues recall for Zantac after confirming the medication can breakdown to create NDMA a known carcinogen. On April 1st, 2020 the FDA issues the following statement. "The U.S. Food and Drug Administration today announced it is requesting manufacturers withdraw all prescription and over-the-counter (OTC) ranitidine drugs from the market immediately. This is the latest step in an ongoing investigation of a contaminant known as N-Nitrosodimethylamine (NDMA) in ranitidine medications (commonly kn

Zantac, an over-the-counter medication used to treat heartburn, may contain low levels of a cancer-causing chemical, according to health officials; however, the U.S. Food and Drug Administration says patients can keep taking Zantac while it investigates how the agent got into the medication. https://cbsn.ws/2O3VEsj | CBS Evening News