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 ...

Magnets embedded in many of Philips’ masks used with CPAP and BiPAP machines could potentially interfere with implanted medical devices, including pacemakers, neurostimulators, metallic stents, ocular ...

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 ...

The DreamStation 2 was not included in Philips’ still-ongoing recall of home respiratory support devices, though the FDA noted that some DreamStation 2s were sent out as replacements for the recalled ...

UPDATE (2024-07-05): Update on Philips Respironics recall of several models of CPAP and BiLevel PAP machines and mechanical ventilators Once consumers have completed the registration process, they ...