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.
Meningitis Outbreak Class Action Lawsuit Filed Over Recalled Injections October 15, 2012 Austin Kirk Add Your CommentsA class action lawsuit has been filed against the compounding pharmacy blamed for a deadly fungal meningitis outbreak, which has been linked to contaminated epidural steroid injections administered to individuals throughout the United States.The case is believed to be the first of what may eventually be hundreds of lawsuits over the meningitis outbreak, as federal health officials are contacting an estimated 14,000 people may have received the recalled injections mixed by the New England Compounding Center (NECC).Barbe Puro filed the complaint (PDF) late last week in the U.S. District Court for the District of Minnesota, seeking class action status to represent all residents of Minnesota who received epidural steroid injections from the compounding pharmacy.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 COMPENSATIONPuro indicates that she received an epidural steroid injection that was from NECC on September 17, and subsequently developed headaches, nausea and other possible symptoms of meningitis. She was later contacted by the Minnesota Department of Health and told to see her physician, because she received an injection that was believed to be contaminated.Although test results have not confirmed whether Puro is one of the more than 200 people nationwide who have been diagnosed with fungal meningitis after receiving the recalled injections, she indicates that she was forced to undergo medical testing, including blood tests and a spinal tap.The meningitis outbreak class action lawsuit was filed on behalf of Puro and all other Minnesota residents who suffered bodily harm, emotional distress or other personal injuries after being injected with doses of contaminated steroids mixed by the New England Compounding Center (NECC).At least six medical providers in Minnesota received the tainted steroids, and the Minnesota Department of Health suggests that about 1,000 residents in the state may have received the injections.Cases of Meningitis from Recalled Steroid Injections Continues to GrowAccording to updated information provided by the CDC on Sunday, infections have been confirmed in 14 different states, including at least 4 in Minnesota. However, the number of diagnosed cases is expected to continue to increase as individuals receiving testing for symptoms of meningitis, as the fungus can be in the body for up to four weeks before symptoms appear.Nationwide, there are now 15 fungal meningitis deaths linked to the injections from NECC, which issued an epidural steroid injection recall on October 3.So far, all of the illnesses have been linked to three lots of preservative-free methylprednisolone acetate solution (MPA), compounded at NECC in Framingham, Massachusetts. The shots are typically injected directly into the spine for pain relief. However, they are also sometimes injected into joints, usually the knee. The CDC reports it has also found several cases of septic arthritis or osteomyelitis of a periperal joint linked to people who were given the MPA injections directly to a joint.The NECC has ceased all operations and recalled all of its injection drugs as a result of the outbreak. The FDA found at least 50 sealed vials of MPA at the pharmacy that contained the fungal contamination believed to be causing the outbreak.Fungal meningitis is a non-contageous form of meningitis caused by mold that somehow tainted vials of the epidural injections. It causes inflammation of the spinal cord and protective membranes covering the brain. The inflammation generally causes an infection of the fluid surrounding the brain and spinal cord and can also be caused by parasites, viruses and bacterial infection. Individuals with a weakened immune system may be at a particularly high risk of contracting fungal meningitis.Symptoms of meningitis following an epidural steroid injection may include fever, headache, stiff neck, nausea, vomiting, increased sensitivity to light and mental confusion.ย As the disease progresses, symptoms may become severe, resulting in seizures, coma and death.In addition to Puro’s class action complaint, NECC is likely to face a number of individual lawsuits over the meningitis outbreak, which have raised concerns about whether the pharmacy has enough insurance or assets to cover the damages caused. Some lawmakers have also suggested that criminal charges should be brought against the pharmacy. Tags: Hospital Infection, Infection, Meningitis, Pharmacy, Pharmacy ErrorMore Lawsuit Stories Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect June 12, 2026 Xcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis June 12, 2026 Rezurock Lawsuit Claims GVHD Medication Caused Debilitating Skin Condition, Prurigo Nodularis June 12, 2026 2 Comments Rachel January 6, 2022 Is this case still open for claims? Richard August 13, 2018 I had a spinal injection back in 2012,and it put me in a chair for 4 years.also it put me in the hospital for 3 days on steroids they said i had a spinal fluid infection. I was unable to go to work anymore. 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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 Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (Posted: yesterday)A spinal cord stimulator lawsuit claims that the Abbott Proclaim XR 5 system failed to treat a manโs chronic pain, instead leaving him with shocks and burning sensations.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026)Lawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (06/02/2026)Spinal Cord Stimulator Malpractice Lawsuit Claims Device Left Veteran Partially Paralyzed (05/29/2026) Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (Posted: 2 days ago)A Suboxone dental erosion lawsuit filed by nine plaintiffs accuses the manufacturer of knowing the film strips caused severe tooth decay and other oral health problems, but failed to warn the medical community or patients.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (05/20/2026)Lawsuit Alleges Suboxone Dental Damage Warnings Were Issued Too Late (05/07/2026)Study Finds No Birth Defect Risks From Suboxone When Compared to Methadone (04/30/2026) Covidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications (Posted: 3 days ago)A Covidien hernia mesh lawsuit will go before a jury next month after a federal judge rejected the manufacturer’s motion to have the case dismissed.MORE ABOUT: HERNIA MESH LAWSUITBard Ventralight Lawsuit Claims Hernia Mesh Failure Resulted in Ongoing Physical Disabilities (06/03/2026)Bard Ventralex Patch Lawsuit Claims Umbilical Hernia Mesh Failed, Requiring Removal Surgery (05/21/2026)Covidien ProGrip Mesh Complications Lawsuit Filed Over Alleged Defects and Failure To Warn Patients (04/21/2026)
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