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.
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.
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.
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
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.
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.
Oculus Recall Issued After Quest 2 VR Headset Foam Causes Skin Reactions, Rashes, Burns July 29, 2021 Luke Tollen Add Your CommentsMillions of Oculus Quest 2 VR headsets are included in a massive recall issued this week, after a removable foam layer has been linked to thousands of reports involving burns, rashes and other skin reactions.The Consumer Product Safety Commission (CPSC) announced the Facebook Oculus Quest 2 VR recall on July 27, indicating the headset foam that pads usersโ faces contains trace elements which can cause skin irritation issues.To date, the manufacturer, Facebook Technologies, LLC, has received at least 5,716 reports of skin irritation, including 45 reports of users needing medical attention.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 COMPENSATIONThe foam interlace included with the Oculus VR headset is meant to prevent a userโs face from directly touching the device, acting as a cushion, while also blocking out exterior light to ensure a better visual experience.Headset foam insert was sold as part of Oculus Quest 2 Virtual Reality devices, as well as sold separately as a โQuest 2 Standard Facial Interface”. The foam is also included in the Quest 2 Fit Pack.The recall affects the Oculus Quest 2, 64 GB, US/TW, Type-A, with SKU 301-00350-01; the Oculus Quest 2 256 GB, US/TW/ Type-A with SKU 301-00351-01; the Oculus Quest 2, Accy, Standard Facial Interface, Global, with SKU 301-00409-01; the Oculus Quest 2, Accy, Fit Pack, Global, with SKU 301-00374-01; and the Oculus Quest 2, Enterprise, 256 GB, US/CA/TW. Type-A, with SKU 301-00402-01. Only headsets and kits with those SKUs are affected by the recall. The SKU and serial number can be found on a label on the packaging of the headset as well as in the userโs account on the Oculus app or on the headset. The affected serial numbers start with โ1WMHHโ and end with numbers below 1264.The devices were sold at BestBuy, GameStop, Target, Walmart, and other retailers while also being sold online on Oculus.com, Amazon.com, BestBuy.com, Gamestop.com, Target.com, and Walmart.com from October 2020 to July 2021 for around $300 to $400. The individual facial interface sold for about $20, and the Fit Pack sold for about $40.The recalled VR headsets were made in China and imported by Facebook Technologies LLC, of Menlo Park, California. A combined total of about 4 million devices sold in the U.S. are impacted, with about 172,600 sold in Canada.Facebook told consumers in April 2021 that its investigation failed to find any contaminants or unexpected substances in the foam. However it did note that foam was found to contain trace substances, normally present in the manufacturing process, which could cause skin discomfort. But the company claims those were at levels below industry standards.The company has suspended sales of the recalled VR headsets until a change in manufacturing has been made to create new foam interlaces for users. Those affected by skin irritation should stop using the foam interlace and all users should contact Facebook Technologies to receive a free silicone cover for the Quest 2 headset and Quest 2 Fit Pack Owners.Consumers with affected headsets can call Facebook Technologies at 877-960-0889 or visit the recall website at https://www.oculus.com/quest-2/removable-facial-interface-alert and click on the Support button for more information. Tags: Allergic Reaction, Facebook, Oculus Quest 2, Skin Irritation, VR Headset RecallMore Lawsuit Stories Jury Selection Underway in First Bard PowerPort Trial Over Infection Claims April 16, 2026 HeartMate II Wrongful Death Lawsuit Claims LVAD Implant Caused Thrombosis April 16, 2026 Video Game Addiction Lawsuit Claims Devs Use Behavioral Manipulation on Kids April 16, 2026 2 Comments Jodi November 3, 2025 My eyes and my forehead is like on fire because of using Oculus 2 what the hell Jennifer April 27, 2024 My child forehead was burn looks really bad using the meta quest 2 CompanyThis 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 Jury Selection Underway in First Bard PowerPort Trial Over Infection Claims (Posted: today)The first Bard PowerPort lawsuit bellwether trial commences next week involving claims that a man suffered a severe infection due to the port catheter’s allegedly defective design.MORE ABOUT: BARD POWERPORT LAWSUITJudge Blocks Juries From Hearing About IVC Filter Problems in Bard PowerPort Trials (04/08/2026)Port-a-Cath Lawsuit Alleges Power P.A.C. Break Down Resulted in Serious Port Catheter Infection (03/31/2026)Final Pretrial Conference in Bard PowerPort Lawsuit To Be Held April 9 (03/27/2026) Hearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (Posted: yesterday)A federal judge has scheduled general causation hearings for Depo-Provera brain tumor lawsuits for June 24 through 26.MORE ABOUT: DEPO-PROVERA LAWSUITHigh-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (04/06/2026)Depo-Provera Meningioma Lawyers Reappointed to MDL Leadership Roles (03/25/2026)Depo-Provera Brain Tumor Symptoms Reported Among Birth Control Users (03/19/2026) WaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (Posted: 2 days ago)A Louisiana man’s Boston Scientific WaveWriter Alpha SCS lawsuit claims the implant failed to provide the promised pain relief and, in fact, made things worse before it needed to be surgically removed.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Neuromodulation Lawsuit Claims Spinal Cord Stimulator Exacerbated Chronic Pain (04/08/2026)Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (04/03/2026)Nevro Spinal Cord Stimulator Lawsuits Filed Over Device Malfunction, Failure (03/30/2026)
Jury Selection Underway in First Bard PowerPort Trial Over Infection Claims (Posted: today)The first Bard PowerPort lawsuit bellwether trial commences next week involving claims that a man suffered a severe infection due to the port catheter’s allegedly defective design.MORE ABOUT: BARD POWERPORT LAWSUITJudge Blocks Juries From Hearing About IVC Filter Problems in Bard PowerPort Trials (04/08/2026)Port-a-Cath Lawsuit Alleges Power P.A.C. Break Down Resulted in Serious Port Catheter Infection (03/31/2026)Final Pretrial Conference in Bard PowerPort Lawsuit To Be Held April 9 (03/27/2026)
Hearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (Posted: yesterday)A federal judge has scheduled general causation hearings for Depo-Provera brain tumor lawsuits for June 24 through 26.MORE ABOUT: DEPO-PROVERA LAWSUITHigh-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (04/06/2026)Depo-Provera Meningioma Lawyers Reappointed to MDL Leadership Roles (03/25/2026)Depo-Provera Brain Tumor Symptoms Reported Among Birth Control Users (03/19/2026)
WaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (Posted: 2 days ago)A Louisiana man’s Boston Scientific WaveWriter Alpha SCS lawsuit claims the implant failed to provide the promised pain relief and, in fact, made things worse before it needed to be surgically removed.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Neuromodulation Lawsuit Claims Spinal Cord Stimulator Exacerbated Chronic Pain (04/08/2026)Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (04/03/2026)Nevro Spinal Cord Stimulator Lawsuits Filed Over Device Malfunction, Failure (03/30/2026)