Zantac Malpractice

Zantac Malpractice Lawyer in Maryland

FDA Requests Removal of All Ranitidine Products

Recently, the FDA requested the removal of Zantac (a ranitidine product), from the market and advised consumers to stop taking the drug.

Zantac and over-the-counter ranitidine contain a carcinogenic contaminant known as N-Nitrosodimethylamine (NDMA).

Exposure to NDMA is known to lead to a number of adverse effects, as well as an increased risk of the following types of cancer:

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