Philips sleep apnea machines, which have been recalled and linked to 500 deaths, are now the subject of a $400 million plus ...
Specifically, certain reworked Philips Respironics Trilogy 100/200 Ventilators, as the FDA has asked for additional safety testing on the silicone foam material used to replace the PE-PUR foam.
The company says: "Philips and Philips Respironics do not admit any fault ... will be for "users of the now-recalled CPAP and other respiratory devices who suffer from significant physical ...
Noninvasive mechanical ventilation (NIV ... The study 2, supported by funding and products by Philips Respironics and ResMed, enrolled 116 patients, randomized to receive either HOT alone ...