The FDA announced that recalled CPAP and BiPAP machines have been tied to hundreds of deaths. The CPAP and BiPAP machines were initially recalled in June 2021. CPAP and BiPAP machines are both worn at ...

The U.S. Food and Drug Administration is alerting patients, caregivers and health care providers that Philips Respironics has recalled certain BiPAP and CPAP masks due to a serious safety concern. The ...

The Philips spokesman said the company "regret [s] the concern that the June 2021 recall notification for specific CPAP, BiPAP and mechanical ventilator devices may have caused for patients and ...

(WKBN) – More than 17 million masks for BiPAP and CPAP machines have been recalled, according to the U.S. Food and Drug Administration. The FDA said that Philips Respironics (Philips) has recalled ...

From May 2022 through July 2022, the FDA received more than 48,000 reports, including 44 reports of death, associated with foam breaking down in recalled devices.

Philips Respironics recalled more than 17 million masks used with their continuous positive airway pressure, or CPAP, and bilevel positive airway pressure, or BIPAP machines.

Health officials report BiPAP and CPAP machines help people with obstructive sleep apnea, respiratory insufficiency or respiratory failure — health conditions that cause pauses in breathing ...