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

The FDA announced today that a Philips recall involving remote cardiac monitoring software is Class I, its most serious ...

The FDA is elevating a recall from Philips related to one of its wearable outpatient heart monitors, used to help detect ...

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

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 ...

The U.S. Food and Drug Administration (FDA) announced on Jan. 13 that Philips is correcting the Monitoring Service Application used with Mobile Cardiac Telemetry Monitoring as some electrocardiogram ...

Abstract: Cardiac monitoring is essential for in-patients with sleep apnea syndrome (SAS), where ... for whole-night BCG and ECG recording using piezoelectric ceramics and Alice 5 polysomnography (PSG ...

The Centers for Medicare & Medicaid Services will review a potential national Medicare coverage policy for renal denervation ...

The "Implantable Loop Recorders Market Size, Share & Trends Analysis Report By Activation, By Application, By End Use, By ...