Respironics Medical Device Recall

Philips Respironics, the manufacturer of DreamStation, System One and Trilogy equipment issued a voluntary product recall on 6/14/21, due to the potential health risks related to sound abatement foam used in specific Philips Continuous Positive Airway Pressure (CPAP), BiLevel Positive Airway Pressure (BiLevel PAP) devices, and Mechanical Ventilators.

For the official notification, click here
For a copy of the recall letter, click here

TO BEGIN THE REGISTRATION PROCESS - CLICK HERE

For questions:

United States: 1-877-907-7508 / Monday to Friday, 8 a.m. to 8 p.m. Eastern Standard Time (U.S.)

Here at CPAP Services, we are committed to assist our patients and help in any way we can. If you have further questions, feel free to call us at 877-488-3800