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

Philips announced a recall for millions of their Bi-Level Positive Airway Pressure (Bi-Level PAP), Continuous Positive Airway Pressure (CPAP), and mechanical ventilator devices in 2021.

Multinational electronics and medical device manufacturer Philips has made headlines ... The largest of these is the FDA class I recall of a series of respirators in 2021 due to the breakdown ...

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 ...

At least two deaths and over a hundred injuries have been linked to a malfunctioning heart monitoring device from Philips and its subsidiary, Braemer. The company affirmed in a statement that that the ...

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

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

During its first-quarter earnings report this spring, Philips, the health technology company, announced it agreed to pay $1.1 billion in a settlement over respiration and sleep apnea machines.

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 ...