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The U.S. Food and Drug Administration is alerting health care professionals and patients of a voluntary recall of 14 lots of prescription ranitidine capsules distributed by Sandoz Inc., used to decrease the amount of acid created by the stomach. This recall is due to a nitrosamine impurity, N-nitrosodimethylamine (NDMA), which was found in the recalled medicine. NDMA is classified as a probable human carcinogen (a substance that could cause cancer).
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You or a loved one may be entitled to compensation if you were exposed to the popular drug Zantac.
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Zantac (Ranitidine) has been being recalled by the FDA for impuriites that have been known to cause cancer. Here is a list of things you should know about this recall and how it affects you.
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