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FDA Requests Removal of All Ranitidine Products (Zantac) from the Market

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 known by the

By |2020-04-04T18:59:57-04:00February 10th, 2020|FDA, In The News, Product Recall|Comments Off on FDA Requests Removal of All Ranitidine Products (Zantac) from the Market

The Impact of E-Cigarettes on the Lung

E-cigarettes are a relatively new tobacco product that have been sold in the U.S. for about a decade The e-cigarettes currently in the U.S. marketplace have not been systemically reviewed by the Food and Drug Administration to determine their impact on lung health. While much

By |2019-09-17T18:36:44-04:00September 15th, 2019|FDA, Products Liability|Comments Off on The Impact of E-Cigarettes on the Lung