Non Veterans

On June 14, 2021 Philips Respironics announced a recall notification (U.S. only) / field safety notice (Outside of U.S) 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.

For information, a complete list of impacted products, potential health risks, and to register your device, please visit philips.com/src-update or call 877.907.7508

If you have a CPAP or Bi-Level device subject to the recall, Phillips Respironics is recommending that you stop using the machine and consult with your physician as to whether or not you should continue to use the machine. The risk of not using the machine may outweigh the risk of continuing to use it. This decision is to be made by you and your physician.

If you have a Ventilator subject to the recall, Respironics advises that you keep using the device and consult with your physician immediately.