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<oembed><version>1.0</version><provider_name>CLP Blog</provider_name><provider_url>https://clpblog.citizen.org</provider_url><author_name>Brian Wolfman</author_name><title>Check out this investigative report on FDA's adverse-event reporting system for medical devices - CLP Blog</title><type>rich</type><width>600</width><height>338</height><html>&lt;blockquote class="wp-embedded-content" data-secret="85qX97Gfkb"&gt;&lt;a href="https://clpblog.citizen.org/check-out-this-investigative-report-on-fdas-medical-device-reporting-system/"&gt;Check out this investigative report on FDA&#x2019;s adverse-event reporting system for medical devices&lt;/a&gt;&lt;/blockquote&gt;&lt;iframe sandbox="allow-scripts" security="restricted" src="https://clpblog.citizen.org/check-out-this-investigative-report-on-fdas-medical-device-reporting-system/embed/#?secret=85qX97Gfkb" width="600" height="338" title="&#x201C;Check out this investigative report on FDA&#x2019;s adverse-event reporting system for medical devices&#x201D; &#x2014; CLP Blog" data-secret="85qX97Gfkb" frameborder="0" marginwidth="0" marginheight="0" scrolling="no" class="wp-embedded-content"&gt;&lt;/iframe&gt;&lt;script type="text/javascript"&gt;
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</html><description>The Minneapolis Star Tribune has published this investigative report&#xA0;on the FDA's adverse-event reporting system for medical devices. The Star Tribune used the Freedom of Information Act to get information from the FDA about patient injuries associated with medical devices. By law, this information should have been public in the first place. The report is quite [...]</description></oembed>
