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.
Central Line Infections Can Be Reduced by Replacing Connectors: Study September 19, 2013 Irvin Jackson Add Your CommentsNew research suggests that the number of central line blood infections at hospitals throughout the United States could be significantly reduced if medical providers did a better job changing the connector in patient IV systems.According to the findings of a study conducted by researchers at Georgia Regents University, use of zero fluid displacement connectors with central line or central catheters that deliver fluids to a patient’s body led to a 60% to 94% drop in central line infection rates.Central line blood infections are a type of healthcare associated infection that affects patients hospitalized and treated for a variety of different conditions. A central line is an intravenous catheter that is inserted directly into a major vein, near to the heart, to draw or transfuse blood or insert medications or fluids. Central line associated blood stream infections (CLABSIs) are infections that are contracted in a hospital setting within a 48-hour window after the central line has been placed.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 COMPENSATIONIt is estimated that 41,000 central line bloodstream infections occur in the U.S. each year, with nearly one in every 20 people hospitalized geting one. The infections usually results in prolonged hospital visits, an increased risk of mortality and increased healthcare costs. The fatality rate can be as high as 25%.According to the researchers, all fluid going through the catheter must go through the connectors, which usually have a positive or negative pressure that pushes fluid out or draws fluid in when they are disconnected for cleaning or flushing. The researchers said that the process of cleaning and flushing the connectors tends to be when infectious bacteria gets into the system.Researchers looked at data in six acute care settings in five states. Using zero-fluid displacement connectors instead of positive pressure connectors led to a 60% drop in central line infections. When negative pressure connectors were replaced with zero-fluid displacement connectors, it eliminated 94% of infections. The connectors cost about $1 each.“We estimate that replacing the connector devices saved about 13 lives in the acute care settings in this study,” said Dr. Cynthia Chernecky, the lead researcher and a Professor of Nursing at Georgia Regents University. “This is a very cost-effective way to increase patient safety.”Central Line Infections PreventableAccording to a 2011ย Consumer Reportsย study, central line infections only account for about 15% of the 1.7 million hospital infections in the U.S. each year, but they are responsible for 30% of the estimated 99,000 hospital infection-related fatalities.In recent years, there has been anย increasing number of hospital infection lawsuitsย filed throughout the United States, as experts believe that most of these potentially life-threatening infections in hospitals can be prevented if steps are taken by the facility and staff.Consumer Reportsย highlighted a checklist developed to reduce the risk of central-line infections. The checklist calls for healthcare professionals to:Wash their hands before, and after examining patients or handling the catheter in any wayDisinfect the patientโs skin before inserting the catheter and during dressing changesUse full-barrier precautions, including mask, cap, gown and gloves and covering the patient with a sterile sheetAvoid groin catheters if possible, as it is one of the most difficult areas to keep clean.Regularly evaluate the need for catheters and remove them when unnecessary. 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: Central Line Infection, Hospital Infection, Infection Image Credit: |More Lawsuit Stories Omnipod Recall Impacts Another 7 Million Defective Pods That May Cause DKA, Hospitalization May 27, 2026 Group of 38 Hair Relaxer Cancer Lawyers Reappointed to MDL Leadership Roles May 27, 2026 Flavored Nitrous Oxide Lawsuit Alleges Amazon Canisters Caused Womanโs Death May 27, 2026 0 Comments NameThis 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 Omnipod Recall Impacts Another 7 Million Defective Pods That May Cause DKA, Hospitalization (Posted: yesterday)Federal regulators have expanded an Omnipod recall after reports that internal tubing defects may cause insulin leaks and under-delivery, potentially triggering dangerous blood sugar spikes.MORE ABOUT: OMNIPOD RECALL LAWSUITRecalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (04/30/2026)Insulet 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) GalaFLEX Mesh Problems May Lead Women To Require Breast Implant Removal Surgery (Posted: 2 days ago)Growing reports of GalaFLEX breast mesh complications have raised concerns about women who required explant surgery, revision procedures or implant removal after the synthetic mesh was used during breast augmentation, breast lift, implant revision or reconstruction surgery.MORE ABOUT: BREAST MESH LAWSUITGalaflex Breast Mesh Lawsuits Filed Against Becton Dickinson in Rhode Island (05/05/2026)Breast Mesh Implant Complications Often Leave Women Asking If They Have a Lawsuit (03/05/2026)Cosmetic Surgeons Warn Against Using Internal Bra Mesh for Breast Lifts (12/11/2025) Depo-Provera Caused Meningioma 29 Years After First Birth Control Shots: Lawsuit (Posted: 6 days ago)Pfizer continues to face Depo-Provera lawsuits from across the U.S., including one by a woman who says she learned of her brain tumor nearly 30 years after she stopped receiving the injections.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Lawsuit Filings Exceed 6,000, As Court Prepares for First Test Trials (05/18/2026)Intracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (05/12/2026)Lawsuit Blames Depo Shot for Brain Tumors, Intense Headaches (04/28/2026)
Omnipod Recall Impacts Another 7 Million Defective Pods That May Cause DKA, Hospitalization May 27, 2026
Omnipod Recall Impacts Another 7 Million Defective Pods That May Cause DKA, Hospitalization (Posted: yesterday)Federal regulators have expanded an Omnipod recall after reports that internal tubing defects may cause insulin leaks and under-delivery, potentially triggering dangerous blood sugar spikes.MORE ABOUT: OMNIPOD RECALL LAWSUITRecalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (04/30/2026)Insulet 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)
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