The government watchdog analyzed about 153 million radiology claims from a five-year period for its new report to Congress, with lawmakers now advocating for change.
Oulu University Hospital lost one of its MRI after relocation and consolidation but was able to maintain output with the help of deep-learning technology.
The money was meant for Minnesota, where criminals were indicted for abusing the Medicaid system to run bogus daycare centers. The Centers for Medicare & Medicaid Services did not specify how the state can rectify the situation to the Trump administration’s satisfaction.
The recall has been designed as the most serious Class I, but the issue can be remedied with a software update. The affected devices are Ivenix Large Volume Pumps, manufactured by Fresenius Kabi.
New research is sounding the alarm on the amount of radiation patients undergoing cardiac imaging are exposed to, prompting experts to call for updated protocols.
The facility in question was not revealed in a video posted on Instagram, where social media star Joshua Cauldwell-Clarke read the letter aloud and asked healthcare workers to please respect the rights of patients.
A civil trial in Maine is underway, where a 71-year-old patient alleges that in 2019, her surgeon read the wrong X-ray, leading to a delayed second procedure that would have put her on the road to recovery.
Researchers from the University of Houston caution that certain implanted electrode cuffs could cause inadvertent stimulation of the nerves during MRI scans.
The government watchdog analyzed about 153 million radiology claims from a five-year period for its new report to Congress, with lawmakers now advocating for change.
![A majority of medical devices involved in Class I recalls were never required by the U.S. Food and Drug Administration (FDA) to undergo premarket or postmarket clinical testing, according to new research published in Annals of Internal Medicine.[1]](/sites/default/files/styles/stack_views/public/2024-09/istock-1209664264.jpg.webp?itok=MzQCOefT)
