November 18, 2019
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The drug company Sandoz Inc., makers of Zantac, has issued a voluntary recall after confirming that the generic Zantac capsules contained an “unexpected impurity, N-Nitrosodimethylamine (NDMA),” which is a probably human carcinogen. The U.S. Food and Drug Administration issued an advisory on Sept. 13, 2019, warning the public of a Zantac cancer risk due to chemical contamination of the heartburn medication. Ring of Fire’s Farron Cousins discusses this with Scott Hardy, President of Top Class Actions.
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