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 ...
Thousands of Philips Respironics’ ventilators are facing issues with inoperative alarms, posing potential risks to patients, the FDA said June 27. The agency said there are reports of 65 deaths and ...
Philips Respironics has recalled bilevel positive airway pressure (BiPAP) ventilators because a false alarm can cause the devices to shut down under certain circumstances. The recall includes Philips’ ...
Two weeks after posting about alarm issues with some Philips Respironics ventilators, the FDA clarified July 10 there have been seven reports of death, not 65. In a June 27 statement, the agency said ...
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 ...
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