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 ...

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 ...

In a classic “two steps forward, one step back” situation, just as Philips is aiming to wrap up the repair-and-replace program for the 5.5 million respiratory devices it began recalling two years ago, ...

Due to a shortage of lifesaving breathing machines amid the COVID-19 (coronavirus) pandemic, the U.S. Food and Drug Administration (FDA) issued guidelines last month that allow hospitals, universities ...

In less than a month, engineers at Sandia National Laboratories converted 100 respiratory machines New Mexico hospitals had on hand into machines that can safely be used as ventilators to treat ...

The US Food and Drug Administration issued a Class I recall Friday, the most serious type of recall, for certain Philips Respironics DreamStation1 CPAP machines. A Class I recall means the FDA has ...

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 ...

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This is an archived article and the information in the article may be outdated. Please look at the time stamp on the story to see when it was last updated. California Gov. Gavin Newsom responded ...

CNN — The US Food and Drug Administration issued a Class I recall Friday, the most serious type of recall, for certain Philips Respironics DreamStation1 CPAP machines. A Class I recall means the FDA ...

Air Voel, Canada’s trusted source for CPAP and sleep therapy devices, announced today that it has expanded its product inventory to now include advanced BiPAP machines designed specifically for ...

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 ...