Do You Qualify for a Philips CPAP Recall Lawsuit in Kentucky?

Request Your Free Consultation

Philips CPAP Recall Lawsuit KentuckyWhile you may have been using a CPAP device and developed cancer, not everyone qualifies for a Philips CPAP recall lawsuit in Kentucky. Below is the current criteria we are following to determine your eligibility:

Am I Eligible to Join a Kentucky Philips CPAP Recall Lawsuit?

If you used any of the following Philips CPAP devices for 6 months or longer and were subsequently diagnosed with cancer, contatc our dangerous drugs and devices attorney immediately: 

All recalled Philips CPAP devices were manufactuared prior to April 26, 2021 and serial numbers are included.

  • SystemOne Q Series
  • DreamStation CPAP, Auto CPAP, BiPAP
  • DreamStation GO CPAP and APAP
  • Dorma 400/500 CPAP
  • REMStar SE Auto CPAP
  • DreamStation ASV
  • DreamStation SV/AVAPS
  • SystemONe ASV4
  • C Series ASV, S/T, AVAPS
  • OmniLab Advanced Plus In-Lab Titration Device
  • E30 Continuous Ventilator
  • Trilogy 100 Ventilator
  • Trilogy 200 Ventilator
  • Garbin Plus, Aeris, LiftVent Ventilator
  • A-Series BiPap Hybrid A30
  • A-Series BiPap V30 Auto
  • A-Series – BiPap V30

Types of Cancer Caused by a Defective Philips CPAP Device in Kentucky

  • Leukemia
  • Breast Cancer
  • Lymphatic Cancer
  • Liver
  • Nasal
  • NHL
  • Lung
  • Brain
  • Multiple Myeloma
  • Prostate
  • Bladder
  • Testicular
  • Stomach
  • Papillary Thyroid Carcinoma
  • Blood
  • Kidney
  • Spleen

Other Non-Cancer Related Illnesses That May Be Eligible

  • Asthma
  • Pulmonary Edema
  • Pulmonary Fibrosis
  • Other Lung Disease
  • Hyper or Hypothryoid Disease
  • Liver Disease/Damage
  • Kidney Disease/Damage

*No cases that have WD or SOL expired will qualify