MDL Sought for Apple Lawsuits Over AirTag Stalking Problems and Damages Caused By Unauthorized Tracking
Scope Infection Lawsuit Patients across the United States have filed medical scope infection lawsuits after contaminated endoscopes and duodenoscopes allegedly transmitted dangerous bacterial infections during procedures such as ERCP, colonoscopy, and other endoscopic treatments.
Spinal Cord Stimulator Lawsuit Spinal cord stimulator lawsuits allege that implanted pain devices malfunctioned, migrated, or caused nerve damage, often forcing patients to undergo revision or removal surgery.
Chlorpyrifos Parkinsonโs Disease Lawsuit Chlorpyrifos lawsuits are being investigated for individuals diagnosed with Parkinsonโs disease after direct, residential, occupational or Gulf War pesticide exposure.
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.
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.
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.
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.
Breast Mesh Lawsuit Lawyers are investigating breast mesh lawsuits for women who suffered infections, pain, or implant failure from internal bra implants used in breast reconstruction surgery.
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.
Subaru Recall Issued Over Air Pump Overheating, Fire Risk November 1, 2016 Russell Maas Add Your CommentsFederal highway safety officials indicate that more than 100,000 turbo-charged Subaru vehicles are being recalled, due to faulty air injection pump relays that may overheat and melt, with at least one vehicle fire reported in connection with the problem.ย The Subaru air injection pump relay recall was announced by U.S. National Highway Traffic Safety Administration (NHTSA) on October 25, following two warranty claims that suggested the vehicles engines began emitting smoke, with one catching on fire. To date, no injuries have been reported.Subaru of America first notified their relay parts supplier, Fuji Heavy Industries (FHI), after receiving a technical report in April 2011 of a check engine light warning due to air injection pump failure. The supplier opened an investigation and instructed its manufacturer to decrease the contact pressure point on the relays in September 2013.Do You Know about…Spinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONDo You Know AboutโฆSpinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONSubaru and FHI received two subsequent warranty claims from customers in October 2013 and May 2015, indicating heavy smoke began emitting from underneath the engine hood, with one of the vehicles catching on fire. Subaru and FHI collected parts from the two incidents and began investigating the root cause of the overheating components. Due to the severe damage the one reported fire caused to the vehicles engine components, Subaru was only able to recover parts to analyze from one vehicle.FHI reported to Subaru on September 30, 2016, that due to an inappropriate manufacturing process control of the relay which controls the secondary air injection pump, the relay may short and fail to turn off the pump. In this event, the pump will continuously run to the point in which it will overheat and potentially cause an engine fire.Subaru is warning customers that in the event the relay fails and causes the pump to overheat, the check engine warning light will illuminate and occupants may begin to smell a burning odor or smoke and possibly see fire.The recall includes 2009 through 2013 Subaru Forester vehicles, 2008 through 2014 Subaru Impreza models, 2007 through 2009 Subaru Legacy models, and 2007 through 2009 Subaru Outback models. All of the vehicles impacted by the recall are equipped with turbo-charged engines.Subaru has not yet provided a notification schedule but has announced the automaker will begin notifying owners of the issue with instructions on how to schedule an inspection at their local dealer. Dealers will be instructed to replace the secondary air injection pump relay free of charge. Customers with further questions may contact Subaru customer service at 1-800-782-2783 and reference the recall number โWtm-73โ. Written by: Russell MaasManaging Editor & Senior Legal JournalistRussell Maas is a paralegal and the Managing Editor of AboutLawsuits.com, where he has reported on mass tort litigation, medical recalls, and consumer safety issues since 2010. He brings legal experience from one of the nationโs leading personal injury law firms and oversees the siteโs editorial strategy, including SEO and content development. Tags: Auto Recall, Car Fire, SubaruMore Lawsuit Stories Nearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials August 12, 2026 MDL Sought for Apple Lawsuits Over AirTag Stalking Problems and Damages Caused By Unauthorized Tracking August 12, 2026 Recalled LINX Device Caused Recurrence of GERD Symptoms, Requiring Surgical Removal: Lawsuit August 12, 2026 0 Comments PhoneThis field is for validation purposes and should be left unchanged.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 NoPost Comment I authorize the above comments be posted on this pageWeekly 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 TermΔ MORE TOP STORIES Nearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (Posted: today)C.R. 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Recalled LINX Device Caused Recurrence of GERD Symptoms, Requiring Surgical Removal: Lawsuit August 12, 2026
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