All Philips BiLevel PAP devices manufactured before April 26, 2021, under all serial numbers.All Philips CPAP devices manufactured before April 26, 2021, under all serial numbers.The following devices used by residents of Indiana are included in the Philips BiPAP recall: Environmental heat and humidity can advance the degradation process, as can unapproved cleaning methods such as the use of ozone to clean the BiPAP or CPAP machine in Indiana. PE-PUR foam in the recalled Philips BiPAP machines put Indiana patients at risk when it breaks down over time. Other "toxic and carcinogenic effects" including a risk of developing cancer.
Irritation of the eyes, skin and respiratory tract.Indiana persons breathing this air are exposed to toxic and cancer-causing chemicals.Īccording to the Philips CPAP recall, Indiana persons who are exposed to chemical emissions from the foam may result in the following side effects: When the sound abatement foam breaks down, toxic gases and small particles are released into the BiPAP machine's airflow. Over time the PE-PUR foam is prone to degradation. The foam component is made of a substance known as PE-PUR, or polyester-based polyurethane. The company had "received reports of possible patient impact due to foam degradation". It was not until Jthat residents of Indiana became aware of the risk when Philips issued a global CPAP recall for 3-4 million devices. Indiana Residents: Philips BiPAP and CPAP Recall
Numerous patients in Indiana make use of these machines on a daily basis. The purpose of the dangerous foam component, which is known as "sound abatement foam", is to lessen the noise the BiPAP, CPAP and ventilator machines make. The problem was a foam part that could be considered an accessory component. Leading up to that time, the company had evidently received concerning reports from doctors and patients about serious side effects linked to Philips CPAP breathing machines. In April of 2021, Philips referenced problems with its CPAP, BiPAP and mechanical ventilator machines as a "quality issue" in its first quarter report.
The devices included in the Philips breathing machine recall include CPAP (continuous positive airway pressure) machines and BIPAP (bilateral PAP) machines for sleep apnea, as well as life-supporting mechanical ventilators. Among them are a range of breathing machines used to support Indiana patients diagnosed with sleep apnea as well as Indiana patients in need of mechanical life support. Philips is a Dutch medical technology company that manufacturers a wide array of medical devices available in Indiana. Philips Breathing Machines and Ventilators Put Indiana Residents at Risk This page provides a comprehensive look at the Philips CPAP recall for residents of Indiana. Lawyers handling Philips BiPAP recall lawsuits believe Indiana persons and family members of Indiana persons who have developed cancer or another serious side effect may be eligible for significant compensation. The Philips CPAP recall was announced on June 14, 2021, and affects between 3 and 4 million CPAP machines, some of which are in use in Indiana. Critics say the company knew of the cancer risk prior to issuing the Philips BiPAP recall, and Indiana families harmed by this dangerous product are now seeking compensation through Philips CPAP cancer recall lawsuits in Indiana. The Philips CPAP recall comes after the Dutch company received reports from patients about side effects they had suffered. Residents of Indiana have been notified that millions of BiPAP and CPAP breathing machines and mechanical ventilators have been recalled by Philips on account of a risk for cancer and other side effects. Tell us what happened: Send Philips BiPAP Recall Information for Residents of Indiana Philips CPAP Recall Sparks Cancer Worry in Indiana