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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.
Rented Medtronic Surgical Kit Linked to Brain Infection Risk in NH, Mass. September 9, 2013 Irvin Jackson Add Your CommentsState health officials indicate that patients at two different hospitals may have been exposed to a risk of a serious brain infection after coming in contact with potentially contaminated Medtronic neurosurgery tools that were rented and used by both facilities.Last week, it was reported that eight patients treated at Catholic Medical Center in New Hampshire were warned about potential exposure after at least one patient died from Creutzfeldt Jakob Disease (CJD), which is similar to “mad cow” disease.On September 5, the Massachusetts Department of Public Health issued a press release warning that at least five other patients treated at Cape Cod Hospital may have also been exposed to a risk of the brain disease, after it was disclosed that the same Medtronic surgical tools were rented by that hospital.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 surgical kit may have become contaminated after it was used on a patient who later died of CJD, which is only 100% detectable after the patient dies. The prions that cause CJD infections cannot, with certainty, be cleaned off of surgical tools via standard hospital sterilization practices. However, officials say there is very little risk of hospital acquired infection because the surgery was conducted on the infected patient’s spine, not his brain.According to Medtronic, seven of the patients who received warnings were treated with the tools, but officials say six more may also be in danger, even though they may not have come in direct contact with the tools.CJD is a rare disease that attacks the nervous system and deteriorates the brain. About one million people each year are affected worldwide, including about 200 annually in the United States. It is always fatal.In a study published last October inย Archives of Neurology, researchers found that less than one-in-five patients suffering from CJD were correctly diagnosed.Early symptoms can include cognitive problems and rapidly failing memory that progress much faster than Alzheimerโs disease or dementia. Symptoms can also include personality changes, anxiety, depression, lack of coordination and visual problems. In later stages, patients may suffer mental deterioration, involuntary movement, blindness, weakness of extremities, and coma. No treatment or cure has yet been developed. 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: Brain Infection, Creutzfeldt-Jakob Disease, Hospital Infection, Infection, MedtronicMore Lawsuit Stories Depo-Provera Meningioma Warning Update Should Be Added to Birth Control Shot: Lawsuit April 22, 2026 Lyft Driver Assault Lawsuit Claims Rideshare Service Performs Inadequate Background Checks Despite Similar Attacks April 22, 2026 Lawsuit Alleges Unsafe Conditions at Planet Fitness Gym Resulted in Womanโs Injuries April 22, 2026 0 Comments InstagramThis 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 Depo-Provera Meningioma Warning Update Should Be Added to Birth Control Shot: Lawsuit (Posted: yesterday)A Depo-Provera meningioma lawsuit argues that Pfizer had a duty to warn women about scientific evidence linking the birth control shot to potential brain tumor growth yet failed to do so.MORE ABOUT: DEPO-PROVERA LAWSUITHearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (04/15/2026)High-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) Judges Will Consider MDL for Dupixent Cancer Lawsuits Late Next Month (Posted: 2 days ago)A group of federal judges will determine whether all Dupixent cancer lawsuits should be formed into a multidistrict litigation, following oral arguments set for May 28.MORE ABOUT: DUPIXENT LAWSUITDupixent Injections Caused Peripheral T-Cell Lymphoma (PTCL) Diagnosis: Lawsuit (04/06/2026)Link Between Dupixent and CTCL Withheld From Users, Medical Community: Lawsuit (03/31/2026)Drug Makers Agree Dupixent Cancer Lawsuits Should Be Centralized in MDL (03/26/2026) SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation (Posted: 3 days ago)A product liability lawsuit alleges unlicensed Abbott representatives made real-time spinal cord stimulator programming decisions based on a Texas womanโs responses, improperly modifying the device and contributing to her injuries.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITWaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (04/14/2026)Boston 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)
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