(WKBN) – The U.S. Food and Drug Administration issued a safety alert on Tuesday about an “emerging safety issue” with some CPAP machines. According to the FDA, the Philips Respironics’ DreamStation 2 ...

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 ...

STATEN ISLAND, N.Y. — The U.S. Food and Drug Administration (FDA) is urging caution when using a certain Philips CPAP machine, due to possible safety issues. The agency is alerting patients and health ...

Earlier this week, the U.S. Department of Justice, representing the Food and Drug Administration and healthcare technology company Philips came to an agreement to no longer sell their sleep therapy or ...

Philips DreamStation 2 continuous positive airway pressure (CPAP) machines should be monitored for signs of overheating, according to the Food and Drug Administration (FDA). The Philips DreamStation 2 ...