CIPAP & BIPAP
CIPAP & BIPAP Lawsuit
People who suffered cancer, lung problems or other injuries after using a recalled Philips machine may file a Philips CPAP lawsuit for potential compensation. Philips recalled millions of its CPAP, BiPAP and ventilator machines because of potential carcinogen and toxic chemical exposure.
Why Are People Filing Philips CPAP Lawsuits?
People are filing Philips CPAP lawsuits because the polyester-based polyurethane (PE-PUR) sound abatement foam in recalled Philips CPAP, BiPAP and ventilator devices may cause cancer and serious respiratory problems.
Individual injury lawsuits seek compensation for injuries and claim Philips manufactured defective devices but didn’t warn the public of the risk or serious injuries. A handful of class-action lawsuits demand that Philips pay for the cost of replacing CPAP devices.
“The FDA’s investigation further reveals the company’s own internal testing showed the degradation products of PE-PUR foam are toxic and potentially carcinogenic. The company chose to keep using the PE-PUR foam anyway, and did not alert the public to the risk of harm,” Brendan McDonough, an attorney overseeing Philips CPAP litigation with national law firm Weitz & Luxenberg, told Drugwatch.
Defective CIPAP & BIPAP Models
DreamStation ASV
DreamStation ST, AVAPS
SystemOne ASV4
C Series ASV, S/T, AVAPS
OmniLab Advanced Plus In-Lab Titration Device
SystemOne (Q series)
DreamStation CPAP, Auto CPAP, BiPAP
DreamStation GO CPAP, APAP
Dorma 400, 500 CPAP
REMStar SE Auto CPAP
Trilogy 100 Ventilator
Trilogy 200 Ventilator
Garbin Plus, Aeris, LifeVent Ventilator
A-Series BiPAP V30 Auto Ventilator