AN IMPORTANT MESSAGE TO OUR CUSTOMERS WITH RESPIRONIC DEVICES
- Philips Respironics has issued a voluntary recall notification (U.S. only) / field safety notice (International Markets) for specific Philips Continuous Positive Airway Pressure (CPAP), BiLevel Positive Airway Pressure (BiLevel PAP) devices, and Mechanical Ventilators.
- Philips Respironics has advised of potential health risks related to sound abatement foam used in specific devices including some DreamStation CPAPs and informs customers and users of potential impacts on patient health and clinical use related to this issue, as well as instructions on actions to be taken.
- For more information about the 2021 Philips Respironics recall, including which devices are affected, please visit the Philips Respironics website at www.philips.com/src-update or call Philips Respironics at (877) 907-7508.
- If you have questions about how this matter might affect your health or your therapy, please contact your physician.