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.
Chlorpyrifos Parkinsonโs Disease Lawsuit Chlorpyrifos lawsuits are being investigated for individuals diagnosed with Parkinsonโs disease after direct, residential, occupational or Gulf War pesticide exposure.
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.
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.
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.
Antibiotic Resistant CRE Infections Are Emerging Threat, CDC Warns October 13, 2015 Irvin Jackson Add Your CommentsGovernment researchers indicate that the U.S. healthcare system faces a growing threat from antibiotic-resistant “super bugs” that have emerged in recent years, which have already resulted in several hospital infection outbreaks.ย In a report published in the Journal of the American Medical Association (JAMA) on October 5, researchers with the U.S. Centers for Disease Control and Prevention (CDC) indicate that they found higher-than-expected numbers of carbapenem-resistant Enterobacteriaceae (CRE) in some major U.S. cities, suggesting that the drug-resistant infections are an emerging threat.While some cities showed lower-than-expected infection rates, cities like Baltimore, New York and Atlanta raised the overall national incidence rate to 2.93 per 100,000 people. The researchers said that while that rate is still much lower than more common types of infections, it does indicate that CRE infections, more commonly referred to as “super bugs”, appear to be becoming more commonplace.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 COMPENSATIONResearchers gather their data from population and laboratory-based surveillance of CRE among people living in seven U.S. metropolitan areas in 2012 and 2013, finding 599 CRE infection cases during that time period.In addition to the overall incidence rate, researchers found that it appears many of the cases were hospital-acquired infections, and that some hospitals may have accidentally transferred the bacteria between facilities. The findings also suggest that about 9% of cases ended in patient deaths.“Hospitalization around the time of the positive CRE culture was common among cases, with the majority among surviving individuals, resulting in discharge directly to a long-term care facility or a long-term acute care hospital” because the patients are generally older and have other health problems, the CDC researchers noted. “The frequent movement of these individuals across the continuum of care underscores their important role in the interfacility spread of CRE, especially if CRE status is not communicated to accepting facilities as part of the transfer process.”Duodenoscope CRE InfectionsAย number of duodenoscope hospital infection outbreaksย were reported earlier this year, including an outbreak of CRE that occurred at UCLAโs Ronald Reagan Medical Center in February. The outbreak caused at least seven infections, two deaths, and raised concerns that nearly 200 other patients had been placed at risk by duodenoscopes manufactured by Olympus Corp.Duodenoscopesย are used in endoscopic retrograde cholangiopancreatography (ERCP) procedures, but difficulties cleaning the devices between patients have resulted in a number of recent outbreaks of antibiotic-resistant hospital-acquired infections in recent years.The duodenoscope CRE infections have been linked to problems with the โreprocessingโ instructions used to clean the devices for use by another patient. FDA reviewers determined thatย the instructions sent out at the time were inadequate and that even if the recommended steps were followed to clean ERCP endoscopes, flaws in the design may allow them to become easily contaminated.On the same day this latest study was published, the FDA ordered duodenoscope manufacturers to conduct new postmarket surveillance studies to try to better identify infection problems related to the medical scopes.Inย August, the FDA issued a safety communication expanding cleaning instructions for duodenoscopes used in ERCP procedures. Olympus Corp. issued expanded cleaning instructions which were approved by the FDA earlier this year.Several duodenoscope infection lawsuits have already been filed ย against Olympus over theย infections linked to the UCLA outbreak. The complaints allege that design problems that make the scopes especially difficult to clean, placing patients at higher risk of contracting illness. 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: CRE, Duodenoscope, Hospital Infections, InfectionsMore Lawsuit Stories Abbott Spinal Cord Stimulator Lead Problems Caused Burning, Shocks, Lawsuit Alleges October 16, 2026 Olympus Medical Device Warning Letter Follows FDA Inspections of Six Manufacturing Facilities October 16, 2026 Dupixent Cancer Risks Lead Experts to Recommend Skin Biopsies Before Treatment October 16, 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 Abbott Spinal Cord Stimulator Lead Problems Caused Burning, Shocks, Lawsuit Alleges (Posted: yesterday)A Georgia womanโs spinal cord stimulator lawsuit alleges she suffered painful shocks and permanent injuries after an Abbott device’s leads migrated out of position.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITMaster Complaint for Spinal Cord Stimulator Lawsuits Against Boston Scientific to Be Filed (10/12/2026)Abbott and Nevro Spinal Cord Stimulator Lawsuits Centralized in New Federal MDLs (10/05/2026)Spinal Cord Stimulator Lawsuit Alleges Boston Scientific Device Failure Required Removal Surgery (09/29/2026) Dozens File Joint Nitrous Oxide Addiction Lawsuit Against Amazon, Third-Party Retailers (Posted: 2 days ago)A joint nitrous oxide addiction lawsuit accuses Amazon and numerous third-party retailers of knowingly selling nitrous oxide for illegal recreational use.MORE ABOUT: NITROUS OXIDE LAWSUITNitrous Oxide Injury Lawsuit Filed Over B12 Deficiency, Long-Term Side Effects (10/09/2026)Amazon, Online Nitrous Oxide Sellers Face Class Action Lawsuit Over Health and Safety Risks (09/04/2026)Nitrous Oxide Sales Restrictions Pass California Legislature Amid Growing Abuse Concerns (09/02/2026) Fourth Bard PowerPort Bellwether Case Set for Trial Dec. 1, as Third Gets Underway (Posted: 3 days ago)A federal judge has scheduled a fourth Bard PowerPort bellwether trial to begin on December 1, while the third trial is slated to begin on October 13.MORE ABOUT: BARD POWERPORT LAWSUITJudge Clears Bard PowerPort Lawsuit for Trial, Rejecting Motion for Summary Judgment (10/02/2026)Bard PowerPort Infection Lawsuit Set for Third Bellwether Trial to Begin Oct. 13 (09/14/2026)Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (09/09/2026)
Olympus Medical Device Warning Letter Follows FDA Inspections of Six Manufacturing Facilities October 16, 2026
Abbott Spinal Cord Stimulator Lead Problems Caused Burning, Shocks, Lawsuit Alleges (Posted: yesterday)A Georgia womanโs spinal cord stimulator lawsuit alleges she suffered painful shocks and permanent injuries after an Abbott device’s leads migrated out of position.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITMaster Complaint for Spinal Cord Stimulator Lawsuits Against Boston Scientific to Be Filed (10/12/2026)Abbott and Nevro Spinal Cord Stimulator Lawsuits Centralized in New Federal MDLs (10/05/2026)Spinal Cord Stimulator Lawsuit Alleges Boston Scientific Device Failure Required Removal Surgery (09/29/2026)
Dozens File Joint Nitrous Oxide Addiction Lawsuit Against Amazon, Third-Party Retailers (Posted: 2 days ago)A joint nitrous oxide addiction lawsuit accuses Amazon and numerous third-party retailers of knowingly selling nitrous oxide for illegal recreational use.MORE ABOUT: NITROUS OXIDE LAWSUITNitrous Oxide Injury Lawsuit Filed Over B12 Deficiency, Long-Term Side Effects (10/09/2026)Amazon, Online Nitrous Oxide Sellers Face Class Action Lawsuit Over Health and Safety Risks (09/04/2026)Nitrous Oxide Sales Restrictions Pass California Legislature Amid Growing Abuse Concerns (09/02/2026)
Fourth Bard PowerPort Bellwether Case Set for Trial Dec. 1, as Third Gets Underway (Posted: 3 days ago)A federal judge has scheduled a fourth Bard PowerPort bellwether trial to begin on December 1, while the third trial is slated to begin on October 13.MORE ABOUT: BARD POWERPORT LAWSUITJudge Clears Bard PowerPort Lawsuit for Trial, Rejecting Motion for Summary Judgment (10/02/2026)Bard PowerPort Infection Lawsuit Set for Third Bellwether Trial to Begin Oct. 13 (09/14/2026)Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (09/09/2026)