While 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