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

Endovascular grafts recalled due to risk of coating breaking off, entering bloodstream

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

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Healthcare advocacy in 2025: American Society of Echocardiography reviews a busy year

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.

FDA finalizes Class I recall for Medtronic catheters

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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FDA confirms new recall for Johnson & Johnson heart device over safety concerns

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

Whole-body MRI provider Prenuvo loses bid to limit damages in high-profile malpractice case

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.

insurance insurer payment claim denial reimbursement prior authorization

Integrating prior authorization into clinical workflows cuts costs, speeds up decisions

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

IV hospital room intravenous drip solution

Ketamine a safe sedation alternative in the interventional radiology suite

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

healthcare surprise billing statement payment

Insurers fudging payment estimates for radiology services under No Surprises Act

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.

Radiomics model links brain MRI features with neuropsychological changes in Crohn's disease

Researchers hope their findings can help pave the way for more targeted therapies for individuals with Crohn's disease.

Artivion, an Atlanta-based medical device company, has received a Humanitarian Device Exemption (HDE) from the U.S. Food and Drug Administration (FDA) for its AMDS Hybrid Prosthesis designed to treat DeBakey Type 1 dissections when malperfusion occurs. This HDE ensures select patients can be treated with the device before the FDA makes its final approval decision.

First surgical device of its kind granted key FDA exemption

This update helps ensure Artivion's AMDS Hybrid Prosthesis can be used to treat high-risk patients as the FDA makes its final approval decision. The news came as Artivion works to bounce back from a cybersecurity attack that occurred in November.

UnitedHealthcare CEO Shooter NYPD Crime Stoppers

Suspect in murder of UnitedHealthcare CEO arrested in Pennsylvania

Luigi Mangione, 26, was on a Greyhound bus traveling through the area on Monday morning. When he stopped at a McDonald's, an employee recognized him from photos circulated by the NYPD. Mangione had evidence on his person linking him to the crime, police said.

Unlocking efficiency in visible light imaging: It’s all about the box

When it comes to managing and storing clinical videos and images captured with visible-light scope devices, the best option is still the box. Connected, integrated, vendor-agnostic, efficient. The box that stands apart as the top choice among imaging leaders is the PACSgear MDR Video Touch 4K capture device from Hyland Software. Here are five reasons why the MDR—which merges hardware and software—outperforms software-only options in the GI lab and others.

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Cardiovascular Business

Endovascular grafts recalled due to risk of coating breaking off, entering bloodstream

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