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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