Foam breakdown may release certain toxic chemicals into the machine air pathwayĪn estimated 80% of the recalled devise were CPAP and BiPAP machines sold primarily under the DreamStation label, according to the recall information.
Foam degradation issues may cause black particles or debris to be inhaled or swallowed.
Problems with the Philips PE-PUR sound abatement foam may include: Philips ventilators may be used in an ICU, hospital, nursing home or in-home care setting among individuals who require mechanical assistance to breath, providing life-sustaining treatment. They are often set to monitor the breathing of the subject and activate when the user stops breathing or when their breathing decreases below a set number of breaths per minute. They can also be used to help infants breathe when they are born with lungs which are not fully developed.īiPAP machines use two-level positive airway pressure, meaning they help both with inhaling and, unlike CPAP machines, assist in exhaling as well. The Philips CPAP machines are used for the treatment of sleep apnea and some other breathing disorders, pushing air through the nostrils and into the back of the throat by increasing air pressure, which keeps the airways open and prevents both snoring and lapses in breathing during sleep. However, due to problems with the material and design of the breathing machines, this PE-PUR foam may break down and release toxic particles and chemicals directly into the machines air pathways. Recalled Philips DreamStation, CPAP (Continuous Positive Airway Pressure), BiPAP (Bi-Level Positive Airway Pressure) and mechanical ventilator machines were sold with defective PE-PUR sound abatement foam, which was intended to reduce noise and vibrations from the devices. Philips Respironics Recall for DreamStation, CPAP, Bi-PAP and Ventilators
#Philips dreamstation trial
Following coordinated discovery and pretrial proceedings, a series of early trial dates will be held in the Philips DreamStation MDL unless a settlement or other resolution for the litigation is reached.
Savage as part of a multidistrict litigation (MDL)
Since October 2021, all Philips CPAP lawsuits have been centralized in the federal court system before U.S.
More than 15 million Philips DreamStation, CPAP, BiPAP and mechanical ventilator machines sold between 2009 and April 2021 contained defective PE-PUR foam, which exposed users of the sleep apnea machines to health risks.
CPAP lawsuits are being pursued against Philips Respironics, a subsidiary of the Dutch conglomerate Koninklijke Philips, N.V.
There are no fees or expenses unless a recovery is obtained.
Medical Treatment for Symptoms Like Headaches, Breathing Problems, Irritation, Nausea and Vomitingįree consultations and case evaluations are provided by CPAP recall lawyers to help determine whether financial compensation may be available through a Philips Respironics class action lawsuit or individual DreamStation injury lawsuit.
Chronic Asthma, Bronchitis or Pneumonia.
Liver Injury, Kidney Injury, Heart Attack, Stroke or Heart Failure.
Sarcoidosis, Pulmonary Fibrosis or other Lung Disease.
Leukemia, Lymphoma or other Cancer Diagnosis.
Philips Respironics has issued a massive recall for CPAP, Bi-PAP and ventilators sold between 2009 and April 2021, which contained a defective PE-PUR sound abatement, which may degrade and release black particles and chemicals directly into the sleep apnea machine air pathways and the lungs of users.įinancial compensation and settlements may be available through a Philips CPAP machine recall lawsuit for individuals who experienced problems, including: Overview of Philips Respironics DreamStation Lawsuit
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