SPRINGFIELD, Mo. – Philips Respironics recalled specific Continuous Positive Airway Pressure (CPAP), Bilevel Positive Airway Pressure (BiPAP), and Ventilators with a manufacturing date between 2009 ...
The U.S. Food and Drug Administration has updated a recall affecting millions of Philips sleep apnea machines, now saying that they may been linked to at least 561 deaths. The agency, in a statement ...
PHILADELPHIA, June 30, 2021 /PRNewswire/ — The national plaintiffs’ law firm Berger Montague has filed a class action lawsuit against Dutch medical equipment company Philips to protect consumers ...
BiPAP A40 is a new multi-modality bi-level ventilator featuring the first fully automatic ventilation mode, designed to support the smooth transition of treatment from hospital to home Philips ...