And it's very much the single-screen option of the two that the new Philips 49B2U6903CH delivers on a very large scale. This ...

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

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

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

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

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