Philips has experienced thousands of complaints, lawsuits, criminal investigations, and a potential DOJ settlement related to CPAP recalls.
Tag: respiratory equipment
Philips Respironics has been conducting comprehensive testing to address potential health risks related to the PE-PUR sound abatement foam in the devices.Read More
Philips is scrutinizing a recall of its ventilators and respiratory devices from the U.S. FDA.Read More
Inspired by the COVID-19 pandemic, emergency physicians have teamed up with product development firm ROBRADY to create a portable negative-pressure ultra-low particulate air, or ULPA, filtration system.Read More
Vyaire Messenger is a novel mobile application that securely provides patient status information and meaningful clinical insights directly to respiratory therapists via their mobile devices.Read More
Philips announces a repair and replacement program for specific Philips Bi-Level PAP, CPAP, and mechanical ventilators related to a voluntary recall of the PE-PUR sound abatement foam in these devices.Read More