February 15, 2017

GAO Report on Power Morcellators Details Limitations of FDA’s Device Adverse Event Reporting System

Doctors Are Not Likely To Report Patient Harm If Devices Perform as Intended, Study Suggests


The Feb. 8 release of a report from a government watchdog agency detailing factors that caused delays in the FDA’s understanding of a cancer risk posed by laparoscopic power morcellators may spur action to improve the agency’s medical device postm...

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