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.
Hair Relaxer Recalls May Be Required By FDA Ban On Straighteners Containing FormaldehydeFDA decision to ban chemical straighteners that emit formaldehyde comes as thousands of hair relaxer lawsuits are being pursued by women diagnosed with uterine cancer, ovarian cancer and other injuries October 18, 2023 Irvin Jackson Add Your CommentsFederal regulators appear likely to ban all chemical hair straighteners that contain or emit formaldehyde, which could lead to massive hair relaxer recalls next year, amid growing concerns about the risk of cancer and other side effects.The U.S. Food and Drug Administration (FDA) issued a proposed rule this week, which would ban formaldehyde and chemicals that release formaldehyde (FA), such as methylene glycol, from being used in hair relaxer products nationwide.โThese chemicals are used in certain cosmetic products that are applied to human hair as part of a combination of chemical and heating tool treatment intended to smooth or straighten the hair,โ the proposed rule states. โUse of hair smoothing products containing FA and FA-releasing chemicals is linked to short-term adverse health effects, such as sensitization reactions and breathing problems, and long-term adverse health effects, including an increased risk of certain cancers.โThe ban would go into effect in April 2024, and comes as manufacturers already face nearly 6,000 hair relaxer lawsuits brought by women diagnosed with uterine cancer, endometrial cancer, ovarian cancer and other injuries that were allegedly caused by endocrine disrupting chemicals contained in many products widely used by African American women, including Dark & Lovely, Just for Me, ORS Olive Oil Motions, Optimum Care and others.HAIR RELAXER COMPENSATIONDid you or a loved one use hair relaxer products?Uterine cancer, endometrial cancer and ovarian cancer may be caused by chemicals in hair relaxer. See if you are eligible for benefits.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONHAIR RELAXER COMPENSATIONDid you or a loved one use hair relaxer products?Uterine cancer, endometrial cancer and ovarian cancer may be caused by chemicals in hair relaxer. See if you are eligible for benefits.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONCalls for Hair Relaxer RecallsThe ban comes after a series of studies that have identified potential cancer risks with hair relaxers, and years of monitoring by the FDA, which first began working on the proposed hair relaxer ban in 2016. However, some environmental and consumer watchdog organizations, such as the Environmental Working Group, have been calling for a formaldehyde ban for hair relaxers since at least 2011.Concerns about the safety of these widely used products spiked late last year, following the publication of a study that highlighted a link between use of hair relaxer and uterine cancer, finding that frequent use was associated with a 156% increased risk compared to women who did not use hair relaxers.In January 2023, the racial justice group Color for Change launched an online campaign to recall hair relaxer products, calling for consumers to pressure major retailers, such as Giant Food, to sell only non-toxic hair relaxer products. This was followed by similar calls by the feminist U.K. health group, Level Up, for LโOreal to remove Dark & Lovely and other hair relaxer products from the market due to cancer risks.FDA Hair Relaxer Formaldehyde WarningsIn conjunction with the proposed formaldehyde ban, the FDA has released a guide for consumers of hair smoothing products and formaldehyde, discouraging them from using products that contain the chemical.โWhen such products are heated, formaldehyde gas is released into the air,โ the FDA warns. โBreathing in formaldehyde gas can be harmful and cause immediate reactions ranging from irritation of the eyes and throat to coughing, wheezing, or chest pain to chronic or long-term problems such as more frequent headaches, asthma, skin irritation, and allergic reactions, and possibly cancer.โThe agency notes that hair relaxers are required by law to include a list of ingredients, and urges consumers to avoid any such products that do not.October 2023 Hair Relaxer Cancer Lawsuit UpdateGiven common questions of fact and law involved in Dark & Lovely lawsuits, Just for Me lawsuits and other claims being pursued against manufacturers of popular chemical straighteners, the U.S. Judicial Panel on Multidistrict Litigation decided earlier this year to consolidate and centralize allย hair relaxer lawsuits as part of an MDL, or multidistrict litigation, and appointed U.S. District Judge Mary M. Rowland to preside over all pretrial proceedings out of the Northern District of Illinois.Judge Rowland has proposed a series of early trial dates designed to help the parties gauge how juries may respond to certain evidence and testimony that will be repeated throughout the claims.Following the MDL proceedings and any early bellwether trials scheduled by Judge Rowland, if the parties fail to negotiate hair relaxer settlements for individuals diagnosed withย uterine cancer,ย ovarian cancer,ย uterine fibroidsย and other complications, Judge Rowland may later remand each individual lawsuit directly filed in the MDL back to the U.S. District Court where it would have originated for a separate trial. 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: Chemicals, Dark & Lovely, Endometriosis, Formaldehyde, Hair Relaxer, Just for Me, L'Oreal, Ovarian Cancer, Uterine Cancer Find Out If You Qualify for Hair Relaxer CompensationMore Hair Relaxer Lawsuit Stories L’Oreal Execs To Face More Questions Over Dark and Lovely, Hair Relaxer Cancer Risks June 29, 2026 Group of 38 Hair Relaxer Cancer Lawyers Reappointed to MDL Leadership Roles May 27, 2026 10 Hair Relaxer Lawsuits Selected by Court for Early Trial Dates April 7, 2026 0 Comments 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 Dupixent CTCL Studies Highlighted Cancer Risks For Years, Lawsuit Alleges (Posted: today)A Dupixent CTCL lawsuit indicates manufacturers have long known the eczema treatment was linked to an increased cancer risk, but failed to warn doctors or patients.MORE ABOUT: DUPIXENT LAWSUITCTCL Lawsuit Alleges Diagnosis Came After Less Than a Year of Dupixent Use (07/29/2026)Lawsuit Alleges Dupixent Caused Mycosis Fungoides Diagnosis (07/21/2026)Dupixent MDL Judge To Meet With Lawyers for Initial Case Management Conference in October 2026 (06/25/2026) Abbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims (Posted: yesterday)Manufacturer wants the Judicial Panel on Multidistrict Litigation to reject a proposal by a group of plaintiffs to consolidate all federal Abbott spinal cord stimulator lawsuits.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (08/06/2026)Spine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026)Spinal Cord Stimulator Reprogramming Caused Electric Shocks, Worsening Pain: Lawsuit (07/27/2026) AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis (Posted: 4 days ago)A Pennsylvania man has filed an AngioDynamics SmartPort lawsuit alleging catheter defects promoted bacterial growth, causing a severe infection and sepsis only weeks after implantation.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Sepsis Lawsuit Claims Defective SmartPort Implant Caused Infection (07/22/2026)SmartPort Catheter Lawsuit Claims Defective AngioDynamics Port-a-Cath Caused Infection (07/14/2026)Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (07/07/2026)
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