PHILIPS RESPIRONICS RECALL INFORMATION

JUNE 17, 2021 (last updated)
 

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.

On June 14, 2021,  VitalAire was informed by Philips Respironics that they have issued a voluntary recall and safety notice for specific Phillips CPAP, BiLevel PAP and Ventilator Devices due to issues related to the polyester-based polyurethane (PE-PUR) sound abatement foam used in these devices. 

Patient safety is of utmost concern for VitalAire. As authorized distributors, we are closely monitoring the situation with Philips Respironics and waiting to receive specific instructions from Phillips on the Philips Respironics repair/replacement program under development. For more information please review the announcement on the Philips Respironics website. 

Please consult with your physician with any questions you may have regarding continuation of your therapy. We will be communicating with our patients as we receive more information and will update this website notice as Philips Respironics releases details regarding its voluntary recall.