Bilevel positive airway pressure (BiPAP) therapy is often used in the treatment of chronic obstructive pulmonary disease (COPD). COPD is an umbrella term for lung and respiratory diseases that make ...

Philips Respironics is recalling some of its BiPAP machines due to a plastic that can contaminate the machine and cause it to fail, according to the U.S. Food and Drug Administration (FDA). The ...

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 ...

Tesla and SpaceX CEO Elon Musk said he’d be sending desperately needed “FDA-approved ventilators” to hard-hit hospitals across the nation dealing with the coronavirus crisis—but they haven’t been the ...

Get all the latest news on coronavirus and more delivered daily to your inbox. Sign up here. As doctors face a shortage of ventilators that are crucial for treating coronavirus patients with ...

NEW HYDE PARK, N.Y.--(BUSINESS WIRE)--In preparation for potential patient surge and shortage of critical mechanical ventilators for hospitalized COVID-19 patients, a Northwell Health physician, a ...

As the coronavirus pandemic rips through the U.S., governors have made public pleas for more personal protective equipment (PPE) for health care and frontline workers, and for ventilators to help ...

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 ...

Northwell Health said it has started to convert bi-level positive airway pressure machines into ventilators for COVID-19 patients. BiPAP machines usually are used for patients who have chronic ...

CORPUS CHRISTI, Texas — As the number of COVID-19 cases in our country rise, supplies are dwindling. Medical professionals facing a shortage of ventilators in some areas of the country are turning to ...

Almost two full years into its Class I recall of more than 5 million respiratory devices, Philips has wrapped up safety tests covering nearly all of the affected models—and is reiterating its previous ...