Did you or a loved one suffer injuries as a result of using one of Philips Respironics recalled CPAP or BiPAP Sleep Apnea Machines or Ventilators? Find out if you qualify in just a few minutes - you may be entitled to compensation.
Philips Sleep Apnea Machine Investigation
Do You Qualify?
You may be eligible to file a lawsuit if you or someone you love used one of the following recalled devices:
SystemOne Q Series
OmniLab Advanced Plus
Dorma 400, 500
REMStar SE Auto
Trilogy 100, 200
Garbin Plus, Aeris LifeVent
We represent clients in all 50 states and would like to hear from anyone who used a recalled ventilator and was later diagnosed with one of the following injuries:
Reactive Airway Disease (RAD)
Sudden Respiratory Failure leading to another injury such as Heart Attack or Heart Failure
On June 14, 2021, Philips announced a recall to "to mitigate potential health risks related to the sound abatement foam component in certain sleep and respiratory care devices." These devices utilized PE-PUR sound abatement foam which may degrade and the particles could enter the device's air pathway and be ingested or inhaled by the user. This foam also may off-gas certain chemicals that could be harmful to the user.
Products not affected by this recall notification (U.S. only) / field safety notice (International Markets) include:
Trilogy Evo OBM
BiPAP A40 EFL
BiPAP A40 Pro
Omnilab (original based on Harmony 2)
Dorma 100, Dorma 200, & REMStar SE
All oxygen concentrators, respiratory drug delivery products, airway clearance products.
Sandy A. Liebhard is a 1988 graduate of Brooklyn Law School and since that time he has been successfully representing plaintiffs in complex litigations. Mr. Liebhard served on the Plaintiffs’ Executive Committee in In re Initial Public Offering Securities Litigation ($586 million recovery) and was involved in the In re Fannie Mae Securities Litigation, where a $153 million settlement received final approval.
Daniel C. Burke
Daniel C. Burke earned his bachelor’s degree in 1990 from the State University of New York at Albany (B.A., English/History), and earned his J.D. in 1993 from St. John’s University School of Law, where he was a member of St. John’s Journal of Legal Commentary.
Morris Dweck received his J.D. in 2014 from the Benjamin N. Cardozo School of Law. He was awarded a Cardozo Scholarship Award throughout his three years in Law School. His note concerning the rare side effects of drugs and diseases was published by the Cardozo Law Journal of Public Law, Policy and Ethics. Mr. Dweck was named a Rising Star by Super Lawyers in 2016-2018.
Free Case Evaluation
Our goal at RX Injury Help is to connect our readers with the tools to protect themselves against defective drugs and medical devices on the market today. To do that, the online resource guide provided by the attorneys at Bernstein Liebhard LLP offers routinely updated medical information on these dangerous products, as well as relevant updates in the growing litigation of lawsuits that have been filed against their manufacturers. If you or someone you love has been injured as a result of a defective medical device or medication on the market today, our Firm can help you seek compensation for damages these products may have caused you.
Qualify In Minutes.You May Be Entitled To Compensation
Do not stop taking a prescribed medication or using a medical device without first consulting with your doctor. Discontinuing use of a prescribed medication or device without your doctor’s advice can result in injury or death.