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New Jersey-based Datascope Corporation has issued a voluntary recall of the Maquet Intra-Aortic Balloon Pump System 98/98XT. The U.S. Food and Drug Administration officially issued the Class I recall on June 16, 2017. The defective medical device affects 9,194 patients in the United States. The company, located in Wayne, New Jersey, entered the recall after » Read More

Most of us take the U.S. Food and Drug Administration (FDA) for granted. However, a recent issue involving the National Health Service (NHS), a key British organization for citizens seeking medical advice, provides us with reason to be pleased with our American counterpart. The NHS is ignoring the facts related to defective vaginal mesh while » Read More