Important information regarding the recall of certain CPAPs, BiLevel PAPs, and ventilators (including non-invasive and invasive ventilation) manufactured by Philips Respironics.
June 14th, 2021 Philips Respironics Company, makers of Positive Pressure Equipment (CPAP, APAP, BiPAP, and ventilators including non-invasive and invasive ventilation), announced the recall of some units due to possible health concerns related to disintegration of the sound abatement foam (polyester-based polyurethane (PE-PUR)) used inside the units to dampen the noise.
For more information about the recall, click here.
To determine if your device is affected by the recall, click here.
How to Locate the Serial Number on your device, click here.
To register your impacted device, click here.
Patient safety is always our concern. We are working with Philips Respironics daily to ensure adherence to and facilitation with the recall process. We are waiting to receive specific instructions from Philips on the repair/replacement program.
For frequently asked questions, click here.
We recommend consulting with your physician for any questions you may have regarding the continuation of your therapy.
If you have additional questions or concerns, please contact us at 1-800-268-5003 or email@example.com.