FDA to Release Millions of Hidden Records about Medical Device Defects

The International Consortium of Investigative Journalists announced on March 27, 2019 that the Food and Drug Administration (FDA) will soon correct a major flaw its disclosure systems. The FDA had, for nearly 20 years, given manufacturers of medical devices the ability to file quarterly reports of incidents to the FDA in a secret “alternative summary…

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Transvaginal Mesh Reclassified by the FDA for Its Potential Dangers

For years, news stories and studies have discussed the potential dangers of transvaginal mesh, or TVM, when used to fix pelvic organ prolapse (POP). On January 4, 2016, the Food and Drug Administration finally addressed the growing problem by “issu[fusion_builder_container hundred_percent=”yes” overflow=”visible”][fusion_builder_row][fusion_builder_column type=”1_1″ background_position=”left top” background_color=”” border_size=”” border_color=”” border_style=”solid” spacing=”yes” background_image=”” background_repeat=”no-repeat” padding=”” margin_top=”0px” margin_bottom=”0px”…

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