Two implanted heart devices used by patients in end-stage heart failure are now under a strict U.S. Food and Drug ...
The FDA calls this "the most serious type of recall," alerting healthcare providers as well as patients about these products ...
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 ...
The U.S. Food and Drug Administration on Wednesday classified a recall of Boston Scientific's device used to block blood flow ...
People should rely on the well-established Heimlich maneuver to save a choking victim, rather than newfangled "anti-choking" ...
The Biden administration recently launched the Global Health Security Strategy, a new effort to combat the spread of ...
Biological material can build up and obstruct blood flow in heart failure patients supported by the left ventricular assist devices, the FDA said.
Two medical devices that mechanically pump blood to the heart have caused hundreds of injuries and more than a dozen deaths ...
The recall affects the only medical option for many patients with end-stage heart failure who do not qualify for a transplant ...