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 has issued a recall of Abbott's Thoratec heart pumps due to reports of 273 injuries and 14 deaths linked to the ...
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 ...
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 ...
Obsidio Embolic is an FDA cleared, single-use product indicated for the minimally invasive embolization of hypervascular ...
After the FDA issued a public safety notice and sent Exactech a warning letter, the firm agreed to recall shoulder implants due to packaging issues.
New Jersey native Lisa Pisano has gotten a new lease on life, thanks to a combined transplant of a mechanical heart pump and ...
Biological material can build up and obstruct blood flow in heart failure patients supported by the left ventricular assist devices, the FDA said.