Philips sent updated instructions after disclosing problems last year with an alarm that can interrupt treatment for people with obstructive sleep apnea or respiratory insufficiency.

The company also added that the recall doesn’t affect Philips’ ongoing efforts to repair and replace all of the CPAP and BiPAP machines and other ventilators included in the initial 2021 recall.

(RTTNews) - Philips, in an update on earlier announced voluntary CPAP, BiPAP and Mechanical Ventilator recall notification, said Sunday that the US Food and Drug Administration recently conducted ...

Philips originally notified users of this recall on February 10, instructing them to locate their CPAP/BiPAP device's serial number, contact providers about manual pressure resets, and to continue ...

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.

AMSTERDAM (dpa-AFX) - Philips, in an update on earlier announced voluntary CPAP, BiPAP and Mechanical Ventilator recall notification, said Sunday that the US Food and Drug Administration recently ...

November 14, 2021 Amsterdam, the Netherlands – On June 14, 2021, Royal Philips’ (NYSE: PHG, AEX: PHIA) subsidiary, Philips Respironics, initiated a voluntary recall notification* for certain sleep and ...

Several Philips ventilators, CPAP and BiPAP machines were recalled in June 2021. The company is currently working to repair and replace the affected devices.