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 ...
Two implanted heart devices used by patients in end-stage heart failure are now under a strict U.S. Food and Drug Administration recall, after being tied to 273 known injuries and 14 deaths, the ...
The recall affects the only medical option for many patients with end-stage heart failure who do not qualify for a transplant ...
People should rely on the well-established Heimlich maneuver to save a choking victim, rather than newfangled "anti-choking" ...
The U.S. Food and Drug Administration on Wednesday classified a recall of Boston Scientific's device used to block blood flow ...
The Food and Drug Administration (FDA) recently announced that two heart devices, the HeartMate II and HeartMate 3 Left ...
Share on Facebook. Opens in a new tab or window Share on X. Opens in a new tab or window Share on LinkedIn. Opens in a new tab or window A pair of heart devices linked to hundreds of injuries and ...