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CPAP Reactive Airway Disease Lawsuit: Have You or a Loved One Suffered From Reactive Airway Disease After Using A Recalled Philips CPAP, BiPAP or Ventilator Machine?

CPAP Reactive Airway Disease Lawsuit cases settlement claims

If you or a loved one suffered from reactive airway disease after using a recalled Philips CPAP, BiPAP or ventilator machine, you may be entitled to recover compensation from a CPAP reactive airway disease lawsuit case or settlement claim.

A team of medical device injury lawyers and class action attorneys is investigating potential lawsuit cases and settlement claims of individuals who claim to have suffered from reactive airway disease after using a recalled Philips CPAP, BiPap or ventilator machine.

Reactive airway disease is a term sometimes used by doctors (when they are hesitant to make a formal diagnosis) to describe a wide range of lung diseases or respiratory conditions in which the lung’s bronchial tubes overreact to an irritant, causing asthma-like symptoms such as wheezing, coughing and shortness of breath.

CPAP Reactive Airways Disease Lawsuit Cases

Philips CPAP reactive airways disease lawsuit cases and settlement claims potentially being investigated include claims of patients who, after using a recalled Philips CPAP, BiPAP or mechanical ventilator machine (e.g., DreamStation, C-Series, Dorma, OmniLab AdvancedPlus, REMstar, System One, A-Series, Garbin Plus, Aeris, LifeVent or Trilogy ventilators machines), suffered from reactive airways disease:

On June 14, 2021, the FDA announced that Philips was recalling some CPAPs, BiPAPs, and ventilators because of possible health risks, including respiratory concerns, relating to potental inhalation of degraded polyester-based polyurethane foam from recalled machines.

Reactive Airways Disease Signs & Symptoms

Signs and symptoms of reactive airways disease can potentially include:

  • Wheezing
  • Coughing
  • Dyspnea
  • Production of sputum
  • Shortness of breath
  • Breathing difficulties
  • Excess mucus in bronchial tube
  • Swollen mucous membrane in bronchial tube
  • Hypersensitive bronchial tubes
  • Hypersensitive airways
  • Swelling of airway lining
  • Other reactive airway disease symptoms

If you or a loved one suffered from reactive airway disease after using a recalled Philips C-PAP, Bi-PAP or ventilator machine, you may be entitled to compensation from a CPAP reactive airway disease lawsuit case or settlement claim. Contact a medical device injury lawyer to request a free case review.

*If you or a loved one are experiencing health issues, side effects or complications from a medical device or healthcare product, we urge you to promptly consult with your doctor or physician for an evaluation.

**The listing of a company (e.g., Koninklijke Philips N.V. or Royal Philips, Philips North America LLC, or Philips RS North America LLC) or product is not meant to state or imply that the company acted illegally or improperly or that the product is unsafe or defective; rather only that an investigation may be, is or was being conducted to determine whether legal rights have been violated.

***The use of any trademarks, tradenames or service marks is solely for product identification and/or informational purposes.

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