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.
Safety Failures At MD Anderson Led To Fatal “Never Event” Blood Transfusion Infection July 1, 2019 Irvin Jackson Add Your CommentsA federal investigation suggests that safety problems at the MD Anderson Cancer Center resulted in an infection and death following a blood transfusion at the renowned University of Texas hospital.The U.S. Centers for Medicare and Medicaid Services (CMS) released a report (PDF) on June 26, detailing the results of an investigation in a patient’s death, highlighting several problems that resulted in the “never event”, which experts widely agree should not occur under any circumstances.The investigation by CMS was conducted from March 29 to April 5, and May 13 to May 17, following the infection of a leukemia patient in December, after undergoing a blood transfusion. That patient died from the blood transfusion infection, which was caused by contaminated platelets.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 COMPENSATIONThat kind of infection and death is considered a โnever eventโ by medical experts, meaning that if a hospital is taking the proper basic precautions, it should never happen. The fact that the MD Anderson is considered one of the leading cancer hospitals in the United States raised the concerns over a so-called never event occurring there even higher.โNever eventsโ are characterized asย surgical errorsย that should not occur during or after surgical procedures, if the proper standards of medical care are followed.ย These events could include conducting surgery on the wrong patient, operating on the wrong part of a patientโs body or leaving foreign objects, such as sponges or medical equipment, in wounds. These mistakes often lead to further complications following surgery, and cost the health care industry an estimated $1 billion annually.The Statement of Deficiencies by CMS investigators found the handling of patient rights, nursing services, laboratory services and other areas out of compliance at the facility. Investigators looked at 33 patient cases and found hospital failures in 18 of those cases.Many of the concerns focused on the nursing staffing and training at the facility. Investigators found a number of nurses had not completed current annual competency testing or training, and also determined that the facilityโs staffing levels were based on budget and not patient safety and failed to reach minimum recommended levels.The investigators noted the facility was short-staffed on registered nurses for 18 of 21 days reviewed and was short on patient care techs on 17 of 21 days reviewed.On June 25, MD Anderson issued a press release addressing the hospital’s failings, saying that it was dedicated to addressing the problems and improving.โWhile it is unfortunate that the CMS surveys resulted from a patient death, we recognize and embrace the opportunity to further enhance and improve our patient care efforts and robust safety measures,โ the press release states. โWe take this feedback seriously, and we already have implemented changes into our clinical practice.โ 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: Blood, Blood Transfusion, Hospital Infection, Infection, LeukemiaMore Lawsuit Stories NFL Sports Gambling Lawsuit Claims Live Game Data Fueled FanDuel, DraftKings Addiction May 1, 2026 Lawsuit Indicates Dupixent Lymphoma Diagnosis Resulted in Multiple Rounds of Chemotherapy May 1, 2026 Medtronic Azure Lawsuit Claims Pacemaker Caused Heart Arrhythmias May 1, 2026 1 Comments Kathleen August 1, 2019 I would like to talk to someone about my motherโs wrongful death at MD Anderson following a blood transfusion. I donโt know what to do or who to talk to. I have all records and impeccable memory of events and negligence. 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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 NFL Sports Gambling Lawsuit Claims Live Game Data Fueled FanDuel, DraftKings Addiction (Posted: yesterday)A public health advocacy group and two Pennsylvania men have filed a lawsuit against FanDuel, DraftKings and the NFL over the use of data for addictive, live in-game microbets.MORE ABOUT: SPORTS BETTING ADDICTION LAWSUITAppeal Challenges Dismissal of DraftKings Lawsuit Over Gambling Addiction (04/27/2026)BetMGM Lawsuit Alleges Gambling Addictโs โSelf-Exclusionโ Listing Was Not Honored (04/13/2026)DraftKings Settlement Reached in Lawsuit Over MLB Gambling Promotions (04/10/2026) Recalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (Posted: 2 days ago)Insulet is removing certain Omnipod 5 insulin pump pods from use following a surge in reports of insulin delivery failures that raise risks of diabetic ketoacidosis and other serious complications.MORE ABOUT: OMNIPOD RECALL LAWSUITInsulet OmniPod 5 Recall Lawsuits May Be Filed Over Problems Resulting in Diabetic Ketoacidosis, Hospitalization and Death (03/24/2026)Omnipod 5 Insulin Pump Recall Follows Reports of Serious Injuries: FDA (03/20/2026) Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (Posted: 3 days ago)A Florida womanโs lawsuit alleges that Abbott Laboratories and Boston Scientific altered their SCS device batteries, firmware and stimulation features without adequate safety testing approved by the FDA.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITJPML Sets Hearing Over Spinal Cord Stimulator Lawsuit Consolidation for May 28 (04/24/2026)SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation (04/20/2026)WaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (04/14/2026)
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