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Cook Medical endovascular grafts recalled due to risk of coating breaking off, entering patient’s bloodstream.

Customers are urged to examine their inventory, quarantine any unused products and return them to the manufacturer. 

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Healthcare policies have rapidly evolved in recent years, and 2025 was no exception. From payment policies to physician shortages, ASE and other medical societies had plenty to fight for throughout the year.

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There is a risk that these catheters will fail to retain their shape during use, causing procedure delays and creating the risk of an adverse outcome. The FDA first warned users about the issue back in August.

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Three patient deaths have been linked to connectivity issues with these devices. The FDA has classified this as a Class I recall.

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Sean Clifford filed the lawsuit Sept. 24, 2024, in the New York State Supreme Court, contending a radiologist failed to spot signs of a forthcoming stroke.   

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This utilization management tactic disproportionately affects specialties such as diagnostic radiology, radiation oncology and cardiology. 

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As IR procedure volumes continue to climb, coupled with anesthesiology provider shortages, there is growing interest in achieving “deeper, more reliable sedation.” 

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A new analysis claims the “benchmark” qualifying payment amount insurers calculate often “dramatically” understates the actual median in-network rates they are paying for in-network care.  

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Rad AI grabbed the highest ranking, at #19 on the list, achieving 8,710% revenue growth between 2020 and 2023, followed by Aidoc and PocketHealth. 

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Accrediting body IAC said revisions help imaging facilities ensure the safe delivery of MRIs, including when key personnel are located off-site.

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The accelerated exam does not come at the expense of image quality, according to new work published in Academic Radiology

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After looking into the case, officials discovered that a coding error prevented the radiology report, which contained critical findings, from ever being sent to the referring provider.

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Customers are urged to examine their inventory, quarantine any unused products and return them to the manufacturer.