Dupixent Lawsuit Dupixent lawsuits are being investigated for patients who developed rare blood cancers such as cutaneous T-cell lymphoma (CTCL) after receiving injections, alleging that Sanofi and Regeneron failed to warn about the potential risks of immune suppression and delayed cancer diagnosis.
Tabletop Fire Pit Lawsuit Individuals who suffered severe burns, or families who lost a loved one in a tabletop fire pit explosion, may be eligible for financial compensation through a fire pit injury lawsuit.
Sports Betting Addiction Lawsuit Sports betting addiction lawsuits are being investigated for college students and young adults who developed gambling problems after using apps like FanDuel and DraftKings, alleging that the platforms failed to warn about the addictive nature of their features and marketing practices.
Nitrous Oxide Lawsuit Individuals who suffered harm, or families who lost a loved one after using nitrous oxide products may be eligible for financial compensation through a nitrous oxide lawsuit.
Hair Relaxer Lawsuit Regular exposure to chemicals in hair relaxer may cause uterine cancer, ovarian cancer and other injuries. Women diagnosed with cancer may be eligible for settlement benefits.
Depo-Provera Lawsuit Depo-Provera lawsuits are being investigated for women who developed meningioma brain tumors after receiving Depo-Provera birth control shots, claiming that Pfizer failed to adequately disclose side effects.
Ozempic Lawsuit Lawyers are pursuing Ozempic lawsuits, Wegovy lawsuits and Mounjaro lawsuits over gastroparesis or stomach paralysis, which can leave users with long-term gastrointestinal side effects
Suboxone Tooth Decay Lawsuit Lawsuits are being pursued by users of Suboxone who experienced tooth loss, broken teeth or required dental extractions. Settlement benefits may be available.
Change Healthcare Lawsuit Lawyers are reviewing Change Healthcare class action lawsuits for individuals who had their personal information stolen due to the data breach.
Bard PowerPort Lawsuit Serious and life-threatening injuries have been linked to problems with Bard PowerPort. Lawsuits are now being pursued by individuals who suffered injuries from the implantable port catheter fracturing or migrating.
Repaired Philips CPAP Sleep Apnea Machines Have Been Returned to Customers with Potentially Unsafe Silicone Foam FDA has ordered Philips to conduct independent testing of the silicone CPAP foam used to repair recalled sleep apnea machines January 27, 2022 Irvin Jackson Add Your Comments Federal regulators issued updated information this week for consumers impacted by a massive Philips CPAP recall last year, indicating that some repaired sleep apnea machines have already been returned to consumers with a new type of silicone foam, even though the agency still does not have sufficient information to determine whether the fixed CPAP machines pose a risk to patients. More than 15 million Philips DreamStation, CPAP, BiPAP and mechanical ventilators were recalled in June 2021, since they contained a defective polyester-based polyurethane (PE-PUR) sound abatement foam, which has been found to degrade and breakdown, releasing toxic chemicals and debris directly into the machine air pathways. These problems have already been linked to reports of long-term side effects for Philips CPAP users, including respiratory injuries, lung damage and cancer. Stay Up-to-Date About Philips CPAP Recall Lawsuits AboutLawsuits.com sends a weekly digest email with information about recalls, lawsuits and warnings that may impact your family, which will include any new Philips CPAP recall lawsuit updates or developments. "*" indicates required fields Email* SIGN ME UP Δ Learn More Stay Up-to-Date About Philips CPAP Recall Lawsuits AboutLawsuits.com sends a weekly digest email with information about recalls, lawsuits and warnings that may impact your family, which will include any new Philips CPAP recall lawsuit updates or developments. "*" indicates required fields Email* SIGN ME UP Δ Learn More On January 26, the FDA announced a new Philips Trilogy EVO ventilator recall, indicating that the same PE-PUR foam was used in several hundred additional devices and repair kits, which were not included in the original recall. The agency also updated answers to frequently asked questions about the recall on Wednesday, highlighting serious on-going concerns about the safety of repaired Philips CPAP machines, where the manufacturer replaced the PE-PUR foam with a different silicone-based sound abatement foam. During a recent inspection of the Philips manufacturing facility, the FDA discovered information that similar silicone foam used in a device marketed outside the U.S. failed a safety test for the release of certain “chemicals of concern”, which may also enter the machine’s air pathways, potentially causing similar health risks to the PE-PUR foam. “The FDA is aware that patients have already received devices with silicone-based foam as part of the repair and replace program,” the updated FAQ notes. “At this time, the agency does not have sufficient information to conclude whether the silicone-based foam being used in the repaired devices poses any risk to patients in the U.S.” Philips has been required to retain an independent laboratory to perform additional testing to determine what safety risks the repaired CPAP machines with silicone foam may pose for consumers. However, the FDA is not yet recommending that patients who received a repaired device should stop using their sleep apnea machine. “The results from the independent testing are needed to determine if the silicone-based foam used in the repaired devices does in fact present any risks to patients, and the FDA will communicate those results to the public as soon as they are available,” the FDA notes. “Patients who have additional concerns should talk to their health care provider about the plan for their care and treatment.” There are currently thousands of individuals pursuing Philips CPAP lawsuits against the makers of the sleep apnea machines, already alleging they were exposed to an increased of cancer, severe respiratory problems and other health complications after breathing chemicals and gases released as the foam breaks down. Given common questions of fact and law raised in product liability and class action lawsuits over recalled sleep apnea machines filed throughout the federal court system, the litigation has been centralized before Senior U.S. District Judge Joy Flowers Conti in the Western District of Pennsylvania for coordinated discovery and pretrial proceedings, as part of a multidistrict litigation (MDL). Written by: Irvin Jackson Senior Legal Journalist & Contributing Editor Irvin Jackson is a senior investigative reporter at AboutLawsuits.com with more than 30 years of experience covering mass tort litigation, environmental policy, and consumer safety. He previously served as Associate Editor at Inside the EPA and contributes original reporting on product liability lawsuits, regulatory failures, and nationwide litigation trends. Tags: CPAP, Medical Device Recall, Philips, Respiratory, Silicone, Sleep Apnea More Philips CPAP Recall Lawsuit Stories Lawsuits Between Philips and SoClean Over CPAP Machine Problems To Be Trial Ready by July 2025 September 3, 2024 Fairness Hearing For Philips CPAP Recall Medical Monitoring Settlement Set for October July 11, 2024 Philips OmniLab Advanced+ Ventilator Recall Issued Over Loss of Therapy Risks July 1, 2024 0 Comments Share Your CommentsFirst Name*Last NameEmail* Shared Comments*This field is hidden when viewing the formI authorize the above comments be posted on this page Yes No Post Comment I authorize the above comments be posted on this page Weekly Digest Opt-In Yes, send me a weekly email with the latest lawsuits, recalls and warnings. Want your comments reviewed by a lawyer?To have an attorney review your comments and contact you about a potential case, provide your contact information below. This will not be published.Contact Phone #Alt Phone #Private CommentsNOTE: Providing information for review by an attorney does not form an attorney-client relationship.CAPTCHAGA SourceGA CampaignGA MediumGA ContentGA TermCompanyThis field is for validation purposes and should be left unchanged. Δ MORE TOP STORIES Lawsuit Claims Walmart Pressure Cooker Lid Exploded, Causing Burn Injuries (Posted: today) A Walmart pressure cooker lawsuit claims the safety features failed to prevent the lid from being removed while under pressure, leading to an explosion and burn injuries. 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