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.
Home Air Tests For Lumber Liquidator Flooring May Not Provide Useful Info: EPA June 8, 2015 Irvin Jackson Add Your CommentsFederal regulators are questioning the usefulness of home air tests being supplied by Lumber Liquidators, which are promoted as a way for homeowners to test whether the company’s laminate flooring may be releasing harmful levels of toxic gas.ย The Environmental Protection Agency (EPA) has posted a series of questions and answers on Lumber Liquidator laminate flooring, which may release high levels of formaldehyde.In the Q&A, the agency cautions consumers against relying too heavily on tests Lumber Liquidators is supplying to concerned customers.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 COMPENSATIONQuestions over formaldehyde problems with Lumber Liquidators flooring surfaced after a โ60 Minutesโ segment earlier this year, which found that products imported from China and sold in California failed to meet the stateโs formaldehyde emissions standards.Some experts suggest that tens of thousands of homes in the state, and potentially hundreds of thousands of homes and businesses nationwide, may be contaminated with toxic Chinese-made flooring.To address concerns from its customers, Lumber Liquidators began offering free indoor air quality screening to customers who received the flooring in early March. It has sent out thousands of home test kits since them and claims that the tests analyzed to date found that more than 97% indicated that air concentrations of formaldehyde were within World Health Organization (WHO) guidelines.Company officials say customers whose tests showed levels of formaldehyde exceeding the guidelines have been notified by the company. However, the EPA raises doubts about the validity of those tests.“EPA has not taken a position on the Lumber Liquidators testing program but cautions the public that air testing may not provide useful information due to the uncertainties of home air testing, the lack of widely accepted health based standards for formaldehyde levels in indoor air to compare test results, and because air testing does not provide information on specific sources of formaldehyde, such as laminate flooring,” the agency warned. “The ‘normal indoor air’ levels cited in the Lumber Liquidatorsโ letter to its customers originate from a paper published in 2010 entitled Formaldehyde in the Indoor Environment, by Dr. Tunga Salthammer. This document is one of many studies referenced in EPAโs external draft document, Toxicological Review of Formaldehyde Inhalation Toxicity: In Support of Summary Information on the Integrated Risk Information System (IRIS). This draft toxicologial review does not represent a conclusion by the Agency on the safety of formaldehyde levels in homes.”Reports suggest that the Justice Department is likely to file criminal charges against Lumber Liquidators for violations of the Lacy Act, which forbids the import of illegally logged wood. The company removed the flooring from the market last month.The U.S. Consumer Product Safety Commission (CPSC) is also investigating the company. If the CPSC finds that the flooring is unsafe, it could result in a Lumber Liquidators laminate flooring recall.A growing number of Lumber Liquidators class action lawsuits have been filed by consumers who have experienced problems with the company’s Chinese-imported flooring.A panel of federal judges is currently considering whether to consolidate all Lumber Liquidator lawsuits under one judge for pretrial proceedings after hearing oral arguments late last month.The creation of a Lumber Liquidators multidistrict litigation (MDL) would centralize the cases before one judge to reduce duplicative discovery into common issues, avoid conflicting pretrial rulings and serve the convenience of the parties, witnesses and the courts.Formaldehyde is a chemical used to manufacture building materials, resins, household products and is used as an embalming agent. It is classified as a probable carcinogen by the EPA and was determined by the National Academy of Sciences to cause cancer in humans. However, the EPA has never passed regulations which set acceptable formaldehyde gas levels for flooring.Common symptoms of exposure to formaldehyde may include respiratory symptoms, eye, nose and throat irritation, headaches, nausea, chest pain, vomiting and rashes. The chemical has been linked to some forms of cancer and leukemia. Written by: Irvin JacksonSenior Legal Journalist & Contributing EditorIrvin 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: Chinese Flooring, Formaldehyde, Lumber LiquidatorsMore Lawsuit Stories Suboxone Manufacturer Faces Nearly 18,000 Dental Erosion Lawsuits July 9, 2026 Medtronic CapSureFix Pacemaker Lawsuit Claims Device Failed and Could Not Be Safely Removed July 9, 2026 College Student Sports Betting May Cause Mental Health Problems: Study July 9, 2026 0 Comments CommentsThis 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 Suboxone Manufacturer Faces Nearly 18,000 Dental Erosion Lawsuits (Posted: today)Indivior faces nearly 18,000 Suboxone dental erosion lawsuits filed by individuals nationwide who say the opioid addiction treatment caused severe tooth damage.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Dry Mouth Lawsuit Claims Dental Problems Could Have Been Avoided With Sublocade Shot (06/18/2026)Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (06/11/2026)Suboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (05/20/2026) Nevro SCS Lawsuits Warrant Centralization in New MDL: Motion (Posted: yesterday)Plaintiffs have requested that the Judicial Panel on Multidistrict Litigation consolidate all Nevro spinal cord stimulator lawsuits in the Central District of California for pretrial procedures.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITProclaim Spinal Cord Stimulator Lawsuit Follows Infection, Battery Migration Problems (07/06/2026)MDL Sought for Abbott Spinal Cord Stimulator Lawsuits (06/29/2026)Lawsuit Alleges WaveWriter Alpha Spinal Cord Stimulator Problems Caused Burning, Shocking Sensations (06/24/2026) Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (Posted: 2 days ago)An AngioDynamics Vortex port lawsuit alleges the implantable port catheter caused a South Carolina woman to suffer pulmonary embolisms and a serious infection requiring surgical removal.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITAngioDynamics Port Catheter Lawsuit Claims Womanโs SmartPort Implants Caused Multiple Infections (06/23/2026)Xcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis (06/12/2026)Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (06/03/2026)
Medtronic CapSureFix Pacemaker Lawsuit Claims Device Failed and Could Not Be Safely Removed July 9, 2026
Suboxone Manufacturer Faces Nearly 18,000 Dental Erosion Lawsuits (Posted: today)Indivior faces nearly 18,000 Suboxone dental erosion lawsuits filed by individuals nationwide who say the opioid addiction treatment caused severe tooth damage.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Dry Mouth Lawsuit Claims Dental Problems Could Have Been Avoided With Sublocade Shot (06/18/2026)Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (06/11/2026)Suboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (05/20/2026)
Nevro SCS Lawsuits Warrant Centralization in New MDL: Motion (Posted: yesterday)Plaintiffs have requested that the Judicial Panel on Multidistrict Litigation consolidate all Nevro spinal cord stimulator lawsuits in the Central District of California for pretrial procedures.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITProclaim Spinal Cord Stimulator Lawsuit Follows Infection, Battery Migration Problems (07/06/2026)MDL Sought for Abbott Spinal Cord Stimulator Lawsuits (06/29/2026)Lawsuit Alleges WaveWriter Alpha Spinal Cord Stimulator Problems Caused Burning, Shocking Sensations (06/24/2026)
Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (Posted: 2 days ago)An AngioDynamics Vortex port lawsuit alleges the implantable port catheter caused a South Carolina woman to suffer pulmonary embolisms and a serious infection requiring surgical removal.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITAngioDynamics Port Catheter Lawsuit Claims Womanโs SmartPort Implants Caused Multiple Infections (06/23/2026)Xcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis (06/12/2026)Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (06/03/2026)