RECALL ALERT-- FDA Recalls Zantac

On April 1, the FDA announced that it was recalling all prescription and over the counter drugs containing ranitidine, the active ingredient in the popular antacid drug, Zantac. In the summer of 2019, a scientific study showed that a contaminant known as N-Nitrosodimethylamine (NDMA) built up in the drug over a period of time. NDMA is a probable human carcinogen (known to cause cancer). At that time, it was thought the NDMA build-up was minimal, and the low levels were acceptable for human consumption. Now, new studies show that NDMA build-up in ranitidine is more significant, and increases dramatically if the drug is stored at higher temperatures.

If you have Zantac, either prescription or OTC, stop taking it immediately! Please dispose of it properly. Do not flush it down the toilet! The FDA has a site explaining how you should dispose of non-flushable drugs, linked here.

If you, a friend or loved one have taken Zantac and had serious side-effects, including a diagnosis of cancer in the stomach, intestines, colorectal, or kidney, give us a call today. We want to help you get the compensation you deserve. Call our offices today, (205) 582-8000.