Physicians would be required to report to the FDA on adverse events caused by medical devices

Frank Interlichia of Rochester joined other patient advocates to celebrate the introduction of House legislation they hope will lead to swifter action by the Food and Drug Administration to take dangerous medical devices off the market.
The two bipartisan bills would make it easier for patients victimized by faulty devices to sue the manufacturers. They also would require physicians to tell the FDA about any problems the devices cause for patients.
Under current law, only hospitals and manufacturers are required to relay such information to the FDA, which patient advocates say leads to serious under-reporting. Physicians already are required to tell the FDA about adverse effects of prescription drugs, using an online database.

http://www.democratandchronicle.com/story/news/2016/06/08/bill-aims-crack-down-dangerous-medical-devices/85626112/

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