Philips Respironics Recall: Philips Respironics announced a voluntary recall for continuous and non-continuous ventilators, and certain CPAP, Bi-Level PAP and ventilator devices due to two issues related to the polyester-based polyurethane (PE-PUR) sound abatement foam used in these devices. To get your machine repaired or replaced, register your device and start your claim at https://www.philipssrcupdate.expertinquiry.com/ For additional information or for patients that do not have access to the internet to register your device, contact Philips Respironics at 877-907-7508.
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Use of the Pulse Ox testing unit. After test completion we will download the equipment and fax a copy of the results to your physician. Test must be returned within 3 days or will be subject to additional charges.
Having issues with your test?
Follow this link for instructions
https://www.virtuox.net/DynDocs/Documents/920m_plus_patient_instructions.pdf