Philips sent updated instructions related to a problem with bilevel positive airway pressure, or BiPAP, machines that can cause interruption or loss of therapy. Philips recalled three models of BiPAP ...
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 ...
A court has ordered the Dutch medical device company Philips and its subsidiary, Respironics, to stop making sleep apnea machines in the US until they resolve a slew of manufacturing issues. The case ...
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 ...
Concluding ongoing class action and personal injury litigations, Philips announced it had reached an agreement through mediation under Judge Diane M. Welsh. The deal does not require Philips ...
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 ...
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