Philips Respironics announces voluntary recall of certain CPAP and other devices


Philips Respironics announced a voluntary recall for continuous and non-continuous ventilators (certain CPAP, Bi-Level PAP and ventilator devices) due to two issues related to the polyester-based polyurethane (PE-PUR) sound abatement foam used in these devices.

For information on the recall notice, a complete list of impacted products, and potential health risks, visit here or call 1-877-907-7508 and register your CPAP in the recall process.

Your home medical equipment provider will assist where they can. Continue to check the Philips website for updated information.

Patients using life sustaining medical devices, should consult a doctor before stopping or altering usage.