The Food and Drug Administration announced that Philips recalled the software following 109 reported injuries and two ...

Cardiac device innovations made waves in 2024, with regulatory approvals, clinical breakthroughs, and product launches ...

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 ...

Analysis by GlobalData has identified that innovative cardiovascular devices are driving diversification in the growing ...

Request To Download Free Sample of This Strategic Report @ The report provides in-depth analysis and insights regarding the current global market scenario, latest trends and drivers into global ECG ...

Some electrocardiogram events, such as atrial fibrillation or abnormally rapid heartbeats, over two years were not reviewed ...