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 issued another ventilator recall deemed the most serious type by the FDA as it may cause serious injury or death.

Though the ongoing recall of approximately 5.5 million of Philips’ respiratory devices—the bulk of them CPAP machines—has dominated most of the last year’s headlines about the medtech giant, it’s not ...