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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.

You may be eligible to file a lawsuit if you or someone you love used one of the following recalled devices:

• DreamStation
• SystemOne ASV4
• SystemOne Q Series
• C Series
• OmniLab Advanced Plus
• E30

• Dorma 400, 500
  
• REMStar SE Auto
• Trilogy 100, 200
  
• Garbin Plus, Aeris LifeVent
• A-Series BiPAP

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:

• Cancer
• Kidney Failure
• Reactive Airway Disease (RAD)
  
• Sudden Respiratory Failure leading to another injury such as Heart Attack or Heart Failure

• Liver Failure
• Lung Damage
• Acute Respiratory Distress Syndrome (ARDS)
• New or Worsening Asthma

Free Case Review:

Call: (888) 404-4339

To see if you qualify to file a Philips Ventilator lawsuit, please contact our office today at (888) 404-4339

Contact us today for a free, no-hassle, phone consultation. Learn about your options and let us answer your questions before you decide on a lawyer to represent you.

We have recovered over 3.5 billion dollars for our clients. However, if we don’t win you don’t pay any costs. 

Established in 1993, our firm has the knowledge/experience necessary to bring cases against big pharma and win. We take pride in driving quality results for each client.

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
• Trilogy Evo OBM
• Trilogy EV300
• Trilogy 202
• BiPAP A40 EFL
• BiPAP A40 Pro
• M-Series
• DreamStation 2
• Omnilab (original based on Harmony 2)
• Dorma 100, Dorma 200, & REMStar SE
• All oxygen concentrators, respiratory drug delivery products, airway clearance products.

Free Case Review
Qualify In Minutes

Call Now or Submit Info

(888) 404-4339

Sandy A. Liebhard

Partner

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

Partner

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

Associate

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.

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.

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Bernstein Liebhard LLP

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Phone: (888) 404-4339

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