Two implanted heart devices used by patients in end-stage heart failure are now under a strict U.S. Food and Drug ...
Two medical devices that mechanically pump blood to the heart have caused hundreds of injuries and more than a dozen deaths ...
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 ...
People should rely on the well-established Heimlich maneuver to save a choking victim, rather than newfangled "anti-choking" ...
The Food and Drug Administration (FDA) recently announced that two heart devices, the HeartMate II and HeartMate 3 Left ...
The recall affects the only medical option for many patients with end-stage heart failure who do not qualify for a transplant ...
A pair of heart devices linked to hundreds of injuries and at least 14 deaths has received the FDA’s most serious recall, the agency announced Monday. The recall comes years after surgeons say ...