Feds Launch Criminal Investigation Into ‘AGGA’ Dental Device and Its Inventor
KFF Health News and CBS News recently reported that multiple lawsuits allege the device has led to grievous injuries to patients’ mouths, resulting in loss of teeth.
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Many of the articles produced by KFF Health News result in action from legislators, regulators and even the White House. Here is a list of our public service journalism that had the highest impact.
KFF Health News and CBS News recently reported that multiple lawsuits allege the device has led to grievous injuries to patients’ mouths, resulting in loss of teeth.
The FDA’s interest in the AGGA dental device follows a KHN-CBS News investigation, according to a former agency official.
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But critics say the new policy still leaves some patients exposed to lawsuits and crippling bills.
KHN reported this week that the University of Virginia Health System has filed 36,000 lawsuits against patients the past six years.
A Kaiser Health News investigation, which first appeared in The Washington Post, showed that the University of Virginia Health System has sued patients 36,000 times for more than $106 million.
After journalists investigate, Fresenius, one of the largest dialysis providers in the U.S., has agreed to waive a half-million-dollar bill. Sovereign Valentine, from Plains, Mont., said it’s a “huge relief.”
After reporting by KHN, NPR and CBS, Fresenius has agreed to waive a Montana man’s huge bill for out-of-network dialysis care.
KHN filed multiple Freedom of Information Act requests over months, and the FDA responded Wednesday saying the data about device malfunctions is now publicly available online.
In reaction to an investigation by Kaiser Health News and the Chicago Tribune, the Illinois legislature has passed a new law to impose fines on nursing homes that fail to meet minimum staffing requirements.
In the wake of a KHN investigation, the agency will no longer let device makers file reports of harm outside a widely used public database.
In an interview, FDA Commissioner Scott Gottlieb reacts to a KHN/Fortune investigation of the drawbacks and risks of electronic health records.
The FDA said it might reclassify the widely used devices featured in a recent Kaiser Health News investigation.
The Food and Drug Administration has let medical device companies file reports of injuries and malfunctions outside a widely scrutinized public database, leaving doctors and medical sleuths in the dark.
Patients and doctors got a chance to share their nightmarish experiences with medical bills with President Donald Trump and other top White House officials.
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