PHILIPS RESPIRONICS RECALL,
INFORMATION FOR PATIENTS
Important information regarding certain CPAPs, BiLevel PAPs, and ventilators (including non-invasive and invasive ventilation) manufactured by Philips Respironics. Please read the information below in detail.
Resources
Download our Philips Respironics Recall Patient Brochure
Read the PHILIPS RESPIRONICS RECALL FAQ
On June 14, 2021, medical device manufacturer Philips Respironics issued a Field Safety Notice regarding the recall of several of its respiratory and ventilator device models currently on the market due to the health risks associated with their use.
For full details of the recall including which devices are affected, please visit the Philips Respironics website.
Philips Respironics has advised of potential health risks related to sound abatement foam used in such specific devices 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.
If you have questions about how this matter might affect your health or your therapy, please contact your physician.
Please complete this acknowledgement form to register your affected device as part of the replacement process.
