The Food and Drug Administration announced that Philips recalled the software following 109 reported injuries and two ...
The FDA is elevating a recall from Philips related to one of its wearable outpatient heart monitors, used to help detect ...
The FDA announced today that a Philips recall involving remote cardiac monitoring software is Class I, its most serious ...
Another 109 people reported injuries after using the remote cardiac monitoring software, Modern Healthcare reported. Other pharmaceutical and tech news is on the FDA's drug approval system and a rapid ...