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.
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
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.
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.
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.
Skin Cancer Screening Shows Questionable Results for Early Melanoma Detection: Study August 2, 2016 Irvin Jackson Add Your CommentsGovernment researchers say it is unclear whether screening for skin cancer actually helps reduce the number of deaths from melanoma, due to the high rate of misdiagnosis, which can lead to unnecessary biopsies, adverse events and overtreatment.ย The U.S. Preventive Services Task Force (USPSTF) issued a recommendation statement last week in the Journal of the American Medical Association (JAMA), indicating that there is insufficient evidence to conclude that visual screening for skin cancer actually provides health benefits overall, particularly for non-lethal forms of skin cancer like basal and squamous cell carcinoma.There was a little more evidence that screening for melanoma, a serious and potentially fatal form of skin cancer, helped, but the evidence was inconclusive, according to the task force, which estimated that 76,400 men and women will develop melanoma in the U.S. this year, and 10,100 will die from it.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 COMPENSATIONAt issue is whether the screening finds enough actual cases of melanoma and other forms of skin cancer early enough for effective treatment and to prevent death in the case of melanoma. Those have to be weighed against the number of misdiagnosis cases, complications from treatment that may have been unnecessary and other health risks that come with treating skin cancer.“The potential for harm clearly exists, including a high rate of unnecessary biopsies, possibly resulting in cosmetic or, more rarely, functional adverse effects, and the risk of overdiagnosis and overtreatment,” the task force warned. “The USPSTF concludes that the current evidence is insufficient to assess the balance of benefits and harms of visual skin examination by a clinician to screen for skin cancer in adults.”Indoor Tanning Melanoma ConcernsThe statement follows a study published in JAMA Dermatology in January, which found that the use of indoor tanning appears to be increasing the rate of melanoma diagnosed in women under the age of 30.In that study, melanoma rates overall increased by 74% among indoor tanners compared to people who donโt tan indoors between the ages of 25 to 59.The findings correlate with those of a 2014 study that revealed younger tanners face a higher risk of developing cancer after using indoor tanning beds than compared to tanning outdoors. Teens were more likely to develop basal cell carcinoma at a much earlier age if they used indoor tanning beds.Researchers believe the higher frequency of tanning and younger starting age are contributing factors to women under 30 experiencing increasing rates of melanoma, compared to older women or men.In another study published in 2014, researchers revealed tanning may also be quite addictive for the nations teens and young adults. Repeated exposure to UV light caused a physical dependence and addiction to tanning, explaining why many people who begin tanning frequently continue to tan.Nearly 80% of the women said they had tanned indoors compared to 44% of men. Women under the age of 50 had higher rates of melanoma than men, but men over the age of 50 had higher melanoma rates than women.Another study published in 2013 in JAMA Internal Medicine found young white women are more likely to ignore the risks associated with indoor tanning, placing them at higher risk of developing cancer.Indoor Tanning Restrictions SoughtIn 2013, the FDA assigned new hazard classifications to indoor tanning devices, upgrading them to a moderate risk device, class II, from the earlier classification of low risk, or class I, in an effort to warn indoor tanners of the risk of using the devices.Despite that move, last year the nation’s doctors called on the FDA to place even more stringent regulations on tanning devices.Late last year, the FDA proposed new rules for tanning beds, calling for teens to be restricted and requiring adults to sing frequent waivers to acknowledge the high risk. 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: Cancer Misdiagnosis, Melanoma, Skin Cancer, Tanning BedMore Lawsuit Stories Bard PowerPort Infection Lawsuit Claims Catheter Fractures Harbored Bacteria November 3, 2026 Chlorpyrifos Pesticide Exposure Detected in Infants, Raising New Neurotoxicity Concerns November 3, 2026 Medtronic Insulin Pump Lawsuit Filed Over Recalled MiniMed 600 Series Device November 3, 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 Bard PowerPort Infection Lawsuit Claims Catheter Fractures Harbored Bacteria (Posted: yesterday)An Illinois man’s lawsuit accuses C.R. Bard of using a defective material in its PowerPort port catheter’s construction, causing him to suffer an infection and device failure.MORE ABOUT: BARD POWERPORT LAWSUITFourth Bard PowerPort Bellwether Case Set for Trial Dec. 1, as Third Gets Underway (10/14/2026)Judge Clears Bard PowerPort Lawsuit for Trial, Rejecting Motion for Summary Judgment (10/02/2026)Bard PowerPort Infection Lawsuit Set for Third Bellwether Trial to Begin Oct. 13 (09/14/2026) Abbott Sales Reps Kept Trying to Reprogram Failed SCS Implant: Lawsuit (Posted: 2 days ago)An Abbott SCS Implant lawsuit claims the manufacturers’ sales representatives potentially delayed removal of a failed device due to attempts to try to reprogram it.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Proclaim Elite Lawsuit Alleges Spinal Cord Stimulator Malfunction Worsened Chronic Pain (10/29/2026)Boston Scientific Spectra WaveWriter Lawsuit Alleges Lead Fracture, Migration and Painful Electric Shocks (10/21/2026)Abbott Spinal Cord Stimulator Lead Problems Caused Burning, Shocks, Lawsuit Alleges (10/16/2026) Ozempic Blindness Lawsuit Alleges Novo Nordisk Concealed NAION Risks (Posted: 5 days ago)A woman’s lawsuit accuses Novo Nordisk of ignoring and downplaying risks of vision loss linked to GLP-1 drugs like Ozempic.MORE ABOUT: OZEMPIC LAWSUITGLP-1 Vision Loss Lawsuit Alleges Ozempic Caused Man to Become Legally Blind (10/13/2026)Ozempic Injection Lawsuit Claims Diabetes Medication Caused Vision Loss (09/22/2026)Lawsuit Blames Mounjaro, Ozempic Side Effects for Vision Loss (09/15/2026)
Chlorpyrifos Pesticide Exposure Detected in Infants, Raising New Neurotoxicity Concerns November 3, 2026
Bard PowerPort Infection Lawsuit Claims Catheter Fractures Harbored Bacteria (Posted: yesterday)An Illinois man’s lawsuit accuses C.R. Bard of using a defective material in its PowerPort port catheter’s construction, causing him to suffer an infection and device failure.MORE ABOUT: BARD POWERPORT LAWSUITFourth Bard PowerPort Bellwether Case Set for Trial Dec. 1, as Third Gets Underway (10/14/2026)Judge Clears Bard PowerPort Lawsuit for Trial, Rejecting Motion for Summary Judgment (10/02/2026)Bard PowerPort Infection Lawsuit Set for Third Bellwether Trial to Begin Oct. 13 (09/14/2026)
Abbott Sales Reps Kept Trying to Reprogram Failed SCS Implant: Lawsuit (Posted: 2 days ago)An Abbott SCS Implant lawsuit claims the manufacturers’ sales representatives potentially delayed removal of a failed device due to attempts to try to reprogram it.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Proclaim Elite Lawsuit Alleges Spinal Cord Stimulator Malfunction Worsened Chronic Pain (10/29/2026)Boston Scientific Spectra WaveWriter Lawsuit Alleges Lead Fracture, Migration and Painful Electric Shocks (10/21/2026)Abbott Spinal Cord Stimulator Lead Problems Caused Burning, Shocks, Lawsuit Alleges (10/16/2026)
Ozempic Blindness Lawsuit Alleges Novo Nordisk Concealed NAION Risks (Posted: 5 days ago)A woman’s lawsuit accuses Novo Nordisk of ignoring and downplaying risks of vision loss linked to GLP-1 drugs like Ozempic.MORE ABOUT: OZEMPIC LAWSUITGLP-1 Vision Loss Lawsuit Alleges Ozempic Caused Man to Become Legally Blind (10/13/2026)Ozempic Injection Lawsuit Claims Diabetes Medication Caused Vision Loss (09/22/2026)Lawsuit Blames Mounjaro, Ozempic Side Effects for Vision Loss (09/15/2026)