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.
Catheter-Associated Urinary Tract Infection Problems May Occur Even With Preventative Measures: Study April 23, 2020 Russell Maas Add Your CommentsHealth experts often consider catheter-associated urinary tract infections to be “never” events, which should not happen if the proper standards of medical care are followed. However, the findings of a new study suggest the problems do occur in some instances, even when facilities following guidelines for preventing the infections.In a research letter published this week in the The Journal of the American Medical Association (JAMA), Texas researchers challenge the common classification of catheter-associated urinary tract infections (CAUTI) as never-events, which may result in medicare of third party payers refusing reimbursement for treatments resulting from the infections.A catheter-associated urinary tract infection (CAUTI) occurs when germs or bacteria enter the urinary tract through the urinary catheter. The infections have been associated with increased complications, deaths, healthcare costs, and length of hospital stay, according to the U.S. Centers for Disease Control and Prevention (CDC). They are considered the leading cause of secondary nosocomial bloodstream infections, carrying a mortality rate of approximately 10%.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 COMPENSATIONSince 2001, catheter-associated urinary tract infections (CAUTI) have widely been considered avoidable errors, which should not occur during or after surgical procedures, if the proper standards of medical care are followed. However, the findings of this latest study suggest this may not be a fair classification.Researchers evaluated data on more than 20,000 surgical procedures at the Michael E. DeBakey Veterans Affairs Medical Center from October 1, 2015 through July 30, 2019, where patients required a catheter. The findings suggest long-term catheter exposure is directly associated with an increase in bacterial infections, even when preventative measures are followed.The study identified 16 CAUTI events where the catheters were removed within 48 hours after the procedure, or there was documentation requiring the catheter remain in use for extended periods which adhered to the Surgical Care Improvement Project guidelines of 2005 passed by the CDC.Of the 16 CAUTI events, six patients had the urinary catheter removed within 48 hours and the remaining 10 cases had a medical need for continued catheter use, such as chronic neurogenic bladder, epidural, or the need for strict urinary output measurementsContrary to health regulators classification that CAUTI events should never happen, researchers indicated that only 60% and 75% of CAUTIs are avoidable when appropriate preventive strategies are used.Despite strict adherence to the Surgical Care Improvement Project guidelines, researchers found the most common type of bacterial infection found among the patients was Escherichia coli, followed by Pseudomonas aeruginosa.The study indicates there is clear evidence CAUTI events can be further reduced by ensuring catheters are used only when needed, and the risk of bacterial infection becomes significantly greater if the urinary catheter is required for longer than 48 hours.A previous CDC report indicated there is a 3%-7% increased risk of acquiring a CAUTI each day a urinary catheter remains in place within the hospital setting.Never events is a classification meant to describe events that should never happen if the proper procedural and safety protocols are taken. Typically this term encompasses situations such as 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 never events mistakes often lead to further complications following surgery, and cost the health care industry an estimated $1 billion annually.In 2005 the CDC introduced guidelines to prevent CAUTI events known as the Surgical Care Improvement Project. By 2008, CMS stopped reimbursing hospitals for treatment of CAUTI as part of what it now known as the Hospital-Acquired Condition Reduction Program (HACRP), with the goal of making CAUTIs a never event, and penalizing hospitals for failing to adhere to the CDC guidelines.However, a 2019 study published in The BMJ, found HACRP penalties charged against poor performing hospitals as part of a Medicare infection reduction program have not helped improve patient care.According to the findings, penalized hospitals had more hospital acquired conditions among patients than non-penalized hospitals, with roughly three infections per 1,000 episodes; compared to only one for every 1,000 episodes in non-penalized hospitals. Penalized hospitals were also found to have higher 30-day readmission rates. Written by: Russell MaasManaging Editor & Senior Legal JournalistRussell Maas is a paralegal and the Managing Editor of AboutLawsuits.com, where he has reported on mass tort litigation, medical recalls, and consumer safety issues since 2010. He brings legal experience from one of the nationโs leading personal injury law firms and oversees the siteโs editorial strategy, including SEO and content development. Tags: Catheter, Hospital Infection, InfectionMore Lawsuit Stories Lawsuit Claims Dupixent Cancer Diagnosis Occurred After Only 8 Months of Use June 17, 2026 Roblox, Snapchat, Discord Lawsuit Alleges Platforms Work in Tandem To Exploit Children June 17, 2026 Boston Scientific Pelvic Mesh Lawsuit Claims Advantage System Caused Permanent Injury, Deformity June 17, 2026 0 Comments LinkedInThis 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 Lawsuit Claims Dupixent Cancer Diagnosis Occurred After Only 8 Months of Use (Posted: today)The makers of Dupixent face a CTCL lawsuit by a man who says he developed the rare form of cancer less than a year after beginning treatment with the eczema drug.MORE ABOUT: DUPIXENT LAWSUITRezurock Lawsuit Claims GVHD Medication Caused Debilitating Skin Condition, Prurigo Nodularis (06/12/2026)Dupixent Injection Lawsuits Consolidated in MDL Over CTCL Diagnoses (06/09/2026)Dupixent Injection Lawsuit Alleges Manufacturer Failed to Warn About T-Cell Lymphoma Cancer Side Effects (06/04/2026) Abbott Spinal Cord Stimulator Battery Problems Led to Repeat Surgeries, Lawsuit Claims (Posted: yesterday)Four plaintiffs allege Abbott spinal cord stimulator battery problems, painful malfunctions and other device failures caused worsening symptoms and repeat surgeries after the company made hundreds of changes to its implant systems.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (06/12/2026)Boston 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) Depo-Provera Lawsuit Settlement Agreement May Resolve Eligible Meningioma Claims in MDL (Posted: 2 days ago)A tentative Depo-Provera lawsuit settlement has been announced, vacating the start of the first bellwether trial while details are finalized.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims (06/05/2026)Depo-Provera Caused Meningioma 29 Years After First Birth Control Shots: Lawsuit (05/22/2026)Depo-Provera Lawsuit Filings Exceed 6,000, As Court Prepares for First Test Trials (05/18/2026)
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