Healthy You - Every Day

Recall on Philips CPAP Devices

Important information for people treated for sleep apnea


As your health partner, LVHN would like to make you aware of a voluntary recall issued by Philips for several of its ventilator products. Our goal is to keep you informed and ensure patients using these products receive the treatment they need.

Recalled Philips products 

The recalled Philips products include Bi-Level Positive Airway Pressure (Bi-Level PAP), Continuous Positive Airway Pressure (CPAP) and mechanical ventilator devices. The recall is associated with foam that is used to make the devices quieter. The foam may degrade into particles that can be inhaled by the user or produce certain chemical emissions. The recalls apply to specific, but not all models of CPAP devices. The recall does not apply to CPAP machines made by ResMed or other manufacturers.

How to determine if your device is recalled 

  • Visit for a list of recalled devices.
  • If you registered your device, check your mail (not your email) for information from Philips about the steps you should take.
  • To register your device to be repaired or replaced and to get the latest information, visit
  • Call Philips at 1-877-907-7508 if you cannot access the website.

If your device is on the list of affected devices

LVHN recommends continuing CPAP therapy, pending further information, if you have any of these conditions:

  • Symptomatic obstructive sleep apnea
  • Obstructive sleep apnea and cardiopulmonary disease
  • The need for treatment to maintain a commercial driver’s license

The health risks associated with discontinuing CPAP therapy for patients with these conditions outweigh the potential safety hazards currently reported by Philips associated with the recalled products.

If your device is not on the list of affected devices

Continue CPAP as prescribed. The recall does not apply to you.

If you are unable to determine the make and model of your CPAP machine

Contact the durable medical equipment (DME) company that will have this information on file.

Potential safety hazards Philips has reported 

  • The potential risks of exposure to degraded foam include irritation (skin, eye, and respiratory tract), inflammatory response, headache, asthma, adverse effects to other organs (e.g. kidneys and liver) and cancer-causing affects.
  • The potential risks of exposure to chemical emissions include headache/dizziness, irritation (eyes, nose, respiratory tract, skin), hypersensitivity, nausea/vomiting, toxic and cancer-causing affects.


We’re here for you

If you followed the above steps and still have questions, contact LVHN at 484-884-2833.

Contact LVHN at 484-884-2833

Explore More Articles