March 7, 2019
Zoll Medical Corporation, which received FDA clearance a few years ago for both home and hospital versions of its wearable defibrillator LifeVest, is now dealing with a range of lawsuits and FDA actions over problems with the device. At least two people have died because their vests failed to activate due to an electrical problem, the FDA reports, while local media in Pittsburgh reports that...
February 21, 2014
Fitbit has announced a voluntary recall of the Fitbit Force after a number of users complained of somewhat mysterious bouts of skin irritation, usually occurring a number of weeks after they began wearing the tracker.
"Recently, some Force users have reported skin irritation," Fitbit CEO James Park said in an open letter to customers. "While only 1.7 percent of Force users have reported any type...