Two implanted heart devices used by patients in end-stage heart failure are now under a strict U.S. Food and Drug ...
The recall comes years after surgeons say they first noticed problems with the HeartMate II and HeartMate 3, manufactured by ...
The recall affects the only medical option for many patients with end-stage heart failure who do not qualify for a transplant ...
The FDA calls this "the most serious type of recall," alerting healthcare providers as well as patients about these products ...
The FDA has issued a recall of Abbott's Thoratec heart pumps due to reports of 273 injuries and 14 deaths linked to the ...
The FDA announced Monday that two heart pump products are being recalled after reports of 14 deaths and hundreds of injuries ...
The Food and Drug Administration (FDA) recently announced that two heart devices, the HeartMate II and HeartMate 3 Left ...
Federal health officials said that nearly 14,000 heart devices tied to hundreds of injuries and more than a dozen deaths are ...
The U.S. Food and Drug Administration on Wednesday classified a recall of Boston Scientific's device used to block blood flow ...
The Biden administration recently launched the Global Health Security Strategy, a new effort to combat the spread of ...
Obsidio Embolic is an FDA cleared, single-use product indicated for the minimally invasive embolization of hypervascular ...
Biological material can build up and obstruct blood flow in heart failure patients supported by the left ventricular assist devices, the FDA said.