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 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.

Pulse Oximetry Testing


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.

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