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FDA Covers for Device Makers, Keeps Injuries Under Wraps

By Mesh Medical Device Newsdesk |

Medical Device News Desk, October 20, 2016 ~ The system is supposed to be transparent.   Medical device makers are required to alert the U.S. Food and Drug Administration (FDA) when their products injure consumers or malfunction.  The FDA then theoretically alerts doctors who alert consumers. In rare cases, such as pelvic mesh, the FDA will [continue reading…]

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