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

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 ...

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

Here are three recent recalls reported to the FDA: ...

The Circular Ring 2 features an AFib detection system that should greatly help the device find its space in the smart ring ...

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

BOSSIER CITY, La. - First responders with the Bossier Parish EMS have just received training on some new equipment they ...

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 ...

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 ...

Philips recalls software for mobile cardiac telemetry devices after patient injuries and deaths. Urgent medical device correction issued. Class I recall.