ufsam.blogg.se - Philips respironics

Patient s who have severe obstructive sleep apnea (OSA), are not experiencing any of the above symptoms or have underlying cardiovascular issues are advised to continue using their device as per the advice of our sleep doctors.

Experience headache, upper airway irritation, cough, chest pressure, sinus infections, nausea or vomiting.

See black debris/particles in the circuit, humidifier, tubing or mask.Stop using your device if you experience the following:.Recall: All devices manufactured before ApAll serial numbers Continuous Ventilator, Minimum Ventilatory Support, Facility UseĬontinuous Ventilator, Non-life SupportingĪt this time, the following steps are recommended to ensure safety: The foam degradation may be exacerbated by the use of unapproved cleaning methods, such as ozone.Īs a patient of our Continuous Positive Airway Pressure (CPAP) Clinic identified to have purchased an affected device, we are bringing this recall to your attention. We have recently received a notice from Philips Respironics announcing a voluntary recall for Continuous and Non-Continuous Ventilators (certain CPAP, BiLevel PAP and Ventilator Devices) due to two issues related to the polyester-based polyurethane (PE-PUR) sound abatement foam used in these devices.