A group of four U.S. representatives have crafted legislation that would give the Food and Drug Administration authority to block the introduction of medical devices that are similar to recalled devices, according to a press release from Rep. Edward J. Markey (D-Mass.).
Read the full report in Becker's Hospital Review on the Safety of Untested and New Devices Act of 2012.
Read the full report in Becker's Hospital Review on the Safety of Untested and New Devices Act of 2012.