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