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 ...

Philips’ Shez Partovi said a lot of the company's focus is working to determine how AI can be used to give time back to ...

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 ...

This innovative feature allows automated maternal pulse detection via the Toco MP transducer without the need to monitor maternal SpO 2 or ECG separately. Built-in NST Trace Interpretation ...

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

How Canadians Feel About Becoming '51st US State' Companies that mandate RTO see slower workforce growth, studies show Arnold Schwarzenegger transforms into Santa for 1st movie in 5 years 14 ...

ChromaFlo works with Philips Volcano’s fast, plug-and-play Eagle Eye Platinum digital IVUS catheter, Eagle Eye Platinum ST and Visions PV .018 and .014 catheters. No flushing and no special ...

The Philips Lumify ultrasound device combines innovative transducer technology with a smartphone or tablet app, offering ...