Zantac, all ranitidine products, to be removed from shelves; FDA cites carcinogen concerns
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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
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FDA issues recall for Zantac after confirming the medication can bre…
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FacebookLawsuit Watch
16 reactions | GSK said it agreed to settle another lawsuit in California alleging its discontinued heartburn drug Zantac caused cancer, as the British drugmaker sought to end costly litigation that has weighed on shares https://reut.rs/48LNN9M | Reuters | Facebook
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9.9K views · 85 reactions | OFF THE SHELVES: The FDA has weighed in on the heartburn medication Zantac, saying limited testing shows levels of a carcinogen that are unacceptably high, as Walmart joins other major retailers in suspending sales of Zantac and generic forms of the drug. David Muir reports. https://abcn.ws/2oBL699 | ABC World News Tonight with David Muir | Facebook
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