AirTag Tracking Lawsuit Claims Apple Failed to Provide Adequate Stalking Safeguards for iPhone, Android Users
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.
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.
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.
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 FanDuel Addiction Lawsuit Alleges Targeted Advertising Caused Substantial Gambling Losses August 19, 2026 AirTag Tracking Lawsuit Claims Apple Failed to Provide Adequate Stalking Safeguards for iPhone, Android Users August 19, 2026 Anti-Seizure Drugs Linked to a Quarter of Stevens-Johnson Syndrome Cases August 19, 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 EmailThis 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 FanDuel Addiction Lawsuit Alleges Targeted Advertising Caused Substantial Gambling Losses (Posted: today)A FanDuel addiction lawsuit claims a Pennsylvania man wagered massive amounts of money after being subjected to a tailored promotional campaign designed to exploit his gambling habits.MORE ABOUT: SPORTS BETTING ADDICTION LAWSUITDraftKings Predictions Lawsuit Seeks Refunds for Illegal Sports Betting Losses (08/11/2026)Class Action Lawsuit Claims DraftKings Is Dodging State Gambling Laws (07/31/2026)Lawsuit Claims FanDuel, DraftKings Caused Compulsive Gambling, Addiction and Financial Losses (07/24/2026) Boston Scientific Stimulator Lawsuit Alleges Spine Implant Caused Nerve Damage, Shocks (Posted: yesterday)A spinal cord stimulator lawsuit from a Kentucky man claims his Boston Scientific device was defectively designed, leaving him with permanent nerve damage and wire fragments fused into his bones.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Stimulator Lawsuit MDL Request Opposed by Manufacturer (08/14/2026)Abbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims (08/10/2026)Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (08/06/2026) Covidien Mesh Lawyers to Meet With MDL Judge This Week, Following Landmark Verdict (Posted: 2 days ago)A federal judge has called for a meeting between attorneys representing plaintiffs and defendants in Covidien mesh lawsuits following an $88 million verdict against the manufacturers.MORE ABOUT: HERNIA MESH LAWSUITCovidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (08/05/2026)Hernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)Bard Composix Kugel Hernia Mesh Lawsuit Claims Defective Implant Required Bowel Resection (07/27/2026)
FanDuel Addiction Lawsuit Alleges Targeted Advertising Caused Substantial Gambling Losses August 19, 2026
AirTag Tracking Lawsuit Claims Apple Failed to Provide Adequate Stalking Safeguards for iPhone, Android Users August 19, 2026
FanDuel Addiction Lawsuit Alleges Targeted Advertising Caused Substantial Gambling Losses (Posted: today)A FanDuel addiction lawsuit claims a Pennsylvania man wagered massive amounts of money after being subjected to a tailored promotional campaign designed to exploit his gambling habits.MORE ABOUT: SPORTS BETTING ADDICTION LAWSUITDraftKings Predictions Lawsuit Seeks Refunds for Illegal Sports Betting Losses (08/11/2026)Class Action Lawsuit Claims DraftKings Is Dodging State Gambling Laws (07/31/2026)Lawsuit Claims FanDuel, DraftKings Caused Compulsive Gambling, Addiction and Financial Losses (07/24/2026)
Boston Scientific Stimulator Lawsuit Alleges Spine Implant Caused Nerve Damage, Shocks (Posted: yesterday)A spinal cord stimulator lawsuit from a Kentucky man claims his Boston Scientific device was defectively designed, leaving him with permanent nerve damage and wire fragments fused into his bones.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Stimulator Lawsuit MDL Request Opposed by Manufacturer (08/14/2026)Abbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims (08/10/2026)Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (08/06/2026)
Covidien Mesh Lawyers to Meet With MDL Judge This Week, Following Landmark Verdict (Posted: 2 days ago)A federal judge has called for a meeting between attorneys representing plaintiffs and defendants in Covidien mesh lawsuits following an $88 million verdict against the manufacturers.MORE ABOUT: HERNIA MESH LAWSUITCovidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (08/05/2026)Hernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)Bard Composix Kugel Hernia Mesh Lawsuit Claims Defective Implant Required Bowel Resection (07/27/2026)