The multispecialty group—which employs about 500 radiologists—is exploring chapter 11 as it grapples with a heavy debt load. 

After high-risk medical devices go through the initial FDA approval process, it is relatively easy for manufacturers to get updates to those devices approved. New evidence suggests that this policy could be leading to more recalls, especially among cardiovascular devices.  

“Organized medicine is united in support of a long-term payment solution," numerous national and state societies wrote to members of Congress. 

A U.S. judge halted all lawsuits against Johnson & Johnson over allegations that its talc formula products and baby powder contained cancer-causing asbestos, stopping any trials as the company has agreed to settle all claims for billions of dollars.

One official described it as the 'largest-ever coordinated law enforcement action' of its kind.

GE Healthcare received clearance from the U.S. Food and Drug Administration (FDA) for its patient monitoring platform, Carescape Canvas.

Among vulnerable women with BRCA1/2 mutations, about 14% never received this vital exam after the rejection, MSK researchers reported.

A common abortion pill, mifepristone, is still in grave danger of being pulled off the market.