There is a risk of the devices sending a reduced amount of energy to the heart during defibrillation. More than 7,000 devices are being recalled due to this issue.

Both conditions are fairly common in patients who undergo TAVR. Is this something cardiologists should be keeping in mind? 

There have been 30 complaints so far about this issue, including 26 injuries and four deaths.

Creating these complex structures with 3D printing alone has never been possible—until now. 

The FDA has categorized this as a Class I recall, which means using the devices “may cause serious injuries or death.”

The new 44-page document focuses on the detection, classification and risk assessment of congenital heart issues.

Researchers tracked data from nearly 38,000 obese patients who underwent TAVR or SAVR, sharing their findings in a new meta-analysis. 

The San Mateo, California-based startup said the money will help it tackle more diseases and add further functions to the company's platform. 

Cheyenne Radiology Group said the incident may have resulted in the inadvertent exposure of patients’ personal information.