** ALL PATIENTS MUST REGISTER THEIR DEVICES **
Philips Respironics announced 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. Philips Respironics is handling the repair and / or replacement of these devices. Equipment received and or delivered from PaO2 has been registered with
PaO2 has registered your unit however you will also need to register
Customers will also need to either call the number listed below or use the link located below to register their unit. Register your unit by providing the serial number located on the bottom of your unit.
Customers will be receiving notice from Respironics regarding this recall. please visit:
Due to this recall by Philips Respironics there is a nationwide shortage of CPAP and Bi-Level PAP devices available.