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 designated 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.
Imaging experts with USC recently shared their observations from the CT imaging of Nes-Hor and Nes-Min—two mummies residing at the California Science Center.
This represents the latest in a series of safety concerns associated with the Impella platform. The FDA said it is still reviewing the matter and will keep the public informed as new details become available.
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)
