FiDA Failed Implant Device Alliance: The New England Journal of Medicine

Joint replacements are the #1 expenditure of Medicare. The process of approving these medical devices is flawed according to the Institute of Medicine. It is time for patients' voices to be heard as stakeholders and for public support for increased medical device industry accountability and heightened protections for patients. Post-market registry. Product warranty. Patient/consumer stakeholder equity. Rescind industry pre-emptions/entitlements. All clinical trials must report all data.

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Twitter: @JjrkCh

Saturday, August 20, 2011

The New England Journal of Medicine - Eliminate 510(k) & track devices.

Public Health Nightmare - Implant "innovation"
published August 10, 2011

"no one's interest is served by putting defective medical devices onto the market where they cause harm to patients, waste health dollars, and may kill jobs when they (device products) are withdrawn."

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6/16/2018 'The Bleeding Edge' documentary screening, Dallas, TX
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9/25/2017 Rally in Washington, DC for the Medical Device Safety Act HR
7/27-29/2017 Leadership Women National Conference, Dallas, TX
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12/1/2016 $1 Billion verdict: J&J DePuy Pinnacle Hip MDL Bellwether Dallas, TX federal jury trial
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Now postponed: RESET to 8/15/2016 from 6/3/2016 Mesh Awareness Movement rally 8am to 11am Edwards v. Ethicon Robert C. Byrd federal courthouse in Charleston, WV
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2/1/2016 to 2/4/2016 CU Safe Patient Project Summit in Washington, DC
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9/21/2015-10/5/2015 Cavness v. JNJ Ethicon Prosima surgical mesh trial, Dallas, TX
6/4/2015-6/6/2015 #Cinderblocks2, The Walking Gallery, Grantsville, MD
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8/21/13 Health and the Built Environment webinar (ReportingonHealth)
7/29/13 PfP CMS Affinity Group webinar
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6/13 & 14/13 PCORI Merit Reviewer
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Saturday, August 20, 2011

The New England Journal of Medicine - Eliminate 510(k) & track devices.

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