Philips CPAP Sleep Apnea Machine Recall

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Philips Bi-Level Positive Airway Pressure (Bi-Level PAP), Continuous Positive Airway Pressure (CPAP), and mechanical ventilator devices were recalled on 6/14/21 after health risks related to lung injury were identified in relation to these devices. Philips estimates 3-4 million devices may be affected.

If you have used the above devices and have experienced any of the following, you may be entitled to monetary compensation:

  • Airway irritation or inflammation
  • Breathing difficulty
  • Colon cancer
  • Heart attack/heart failure
  • Kidney cancer
  • Kidney disease
  • Liver cancer
  • Liver disease
  • Lung cancer
  • Lung damage
  • New or worsening asthma
  • Pneumonia
  • Respiratory failure
  • Stroke

If you have used a Philips CPAP Sleep Apnea machine and have health issues as a result, please fill out the form below for an attorney to review your case and contact you.