Medscape

Philips Respironics Updates Device Use Correction

Philips Respironics has updated use instructions for three bi-level positive airway pressure machines, according to a recall statement posted by the US FDA. The recall does not include removal of the ...
KRQE Blogs

Philips provides update on completed set of test results for CPAP/BiPAP sleep therapy devices

Amsterdam, the Netherlands – Royal Philips (NYSE: PHG; AEX: PHIA), today provides an update on the comprehensive test and research program of its subsidiary Philips Respironics to assess potential ...
WOKV

FDA: Recalled Philips BiPAP, CPAP machines tied to more than 560 deaths

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 ...
FierceBiotech

Philips plots return to US sleep apnea market after final consent decree in CPAP recall

A U.S. federal court has officially ordered Philips to restrict the production and sale of its CPAP and BiPAP ventilators for sleep apnea. The move is the culmination of a years-long international ...
People

Recalled Sleep Apnea Machines Tied to 561 Deaths

Philips CPAP and BiPap machines that were recalled in 2021 have since been linked to deaths and thousands of malfunctions, the FDA says Roberto Machado Noa/LightRocket via Getty The Food and Drug ...
FierceBiotech

FDA collects another 6,000 complaints—including 40 deaths—linked to Philips' CPAP recall

Despite recent test results showing that the disintegrating polyester-based polyurethane (PE-PUR) foam at the heart of Philips ongoing respiratory device recall “is unlikely to result in an ...