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.
Recalled Artificial Tears Eye Drops Linked to Fourth Death, CDC ReportsAt least four patients have also had to have an eye surgically removed due to infections caused by recalled Artificial Tears eye drops, the CDC reports. May 22, 2023 Irvin Jackson Add Your CommentsAmid continuing concerns about bacterial contamination that resulted in an Artificial Tears eye drops recall earlier this year, federal disease experts have confirmed additional reports involving severe infections among users nationwide, and indicate that at least four people have died.The U.S. Centers for Disease Control and Prevention (CDC) issued an update on the Artificial Tears infection outbreak on May 15, indicating that the agency is aware of at least 81 infections linked to the recalled eye drops in 18 different states. In addition to four deaths linked to severe infections that resulted from the eye drops, the agency indicates that a number of other cases involved hospitalization or individuals who suffered vision loss, with at least another four cases resulting in the need for surgical eye removal.The Artificial Tears recall was first issued in February 2023, leading health officials to warn consumers and medical providers to immediately stop using EzricCare and Delsam Pharma Artificial Tears eye drops, which have been found to be contaminated with carbapenem-resistant Pseudomonas aeruginosa.Artificial Tears Infection RecallInformation about the Artificial Tears infection outbreak first surfaced in late January 2023, when the CDC identified a cluster of individuals experiencing bacterial infections after using EzriCare eye drops. This immediately led to calls for a recall, and a steadily growing number ofย Artificial Tears lawsuitsย brought both by individuals diagnosed with infections, as well as consumer class action claims that seek economic damages and medical monitoring.Stay Up-to-Date Abouteye drop recallsAboutLawsuits.com sends a weekly digest email with information about recalls, lawsuits and warnings that may impact your family. "*" indicates required fieldsEmail* SIGN ME UPΔ Learn MoreStay Up-to-Date Abouteye drop recallsAboutLawsuits.com sends a weekly digest email with information about recalls, lawsuits and warnings that may impact your family."*" indicates required fieldsEmail* SIGN ME UPΔ Learn MoreThe recall initially impacted 15 ml bottles of EzriCare Artificial Tears, sold in a blue box, and Delsam Phama Artificial Tears, sold in a white box. However, several weeks later, the FDA expanded the recall to includeย Delsam Pharma Artificial Eye Ointmentย as well.The EzriCare and Delsam Pharma Artificial Tears were sold through Amazon.com, Walmart and other nationwide retails, and have been widely used by consumers for symptoms of dry or itchy eye symptoms, or other eye conditions, such as glaucoma or ocular hypertension. The recalled eye drops were also distributed directly to hospitals, healthcare centers and nursing homes nationwide.CDC investigators began looking at the Artificial Tears products after severalย Pseudomonas aeruginosa outbreaks in nursing homes surfaced in Connecticut and Utah, and have indicated that elderly or infirmed individuals may face the greatest risk. That trend continued in the lastest update, the CDC reports.Health officials indicate that all consumers should be aware of the potential eye infection symptoms, which may include;Yellow, green, or clear discharge from the eyeEye pain or discomfortRedness of the eye or eyelidFeeling of something in your eye (foreign body sensation)Increased sensitivity to lightBlurry visionArtificial Tears Eye Drops LawsuitsAs the number of reported eye drops infections continue to rise, a series ofย eye drops lawsuitsย have been filed in recent weeks, claiming the manufacturers failed to perform proper microbial testing, allowing the products to be sold directly to consumers containing Pseudomonas aeruginosa.The Artificial Tears lawsuits indicate that, as a result, consumers have now suffered eye infections that have resulted in permanent vision loss and other injuries.Lawyers are actively investigating potentialย eye drop infection lawsuitsย against the manufacturers and distributors of EzriCare and Delsam Pharmaโs eye drops for multiple injuries and side effects caused by the contamination, including;Eye InfectionPartial BlindnessPermanent BlindnessBloodstream InfectionOther injuries caused by the eye drops 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: Artificial Tears, Blindness, Eye Infection, Eye Injury, EzriCare Eye Drops, Infection, Vision LossMore Eye Drops Recall Lawsuit Stories Lawsuit Alleges Infection From Recalled Eye Drops Caused Permanent Vision Damage, Light Sensitivity July 8, 2024 Eye Drops Vision Damage Lawsuit Filed Over Bacteria in Recalled Artificial Tears June 7, 2024 Amazon Artificial Tears Lawsuit Filed Over Bacterial Keratitis Infection from Contaminated Eye Drops February 15, 2024 0 CommentsURLThis 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 SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation (Posted: today)A product liability lawsuit alleges unlicensed Abbott representatives made real-time spinal cord stimulator programming decisions based on a Texas womanโs responses, improperly modifying the device and contributing to her injuries.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITWaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (04/14/2026)Boston Scientific Neuromodulation Lawsuit Claims Spinal Cord Stimulator Exacerbated Chronic Pain (04/08/2026)Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (04/03/2026) Passenger in Uber Sexual Assault Trial Tells Jury She Feared Driver Knowing Her Address (Posted: 3 days ago)The second federal Uber sexual assault bellwether trial is underway in North Carolina, involving claims a woman was groped and had to flee from the driver.MORE ABOUT: UBER SEXUAL ASSAULT LAWSUITMDL Judge Appoints Lyft Sexual Assault Lawyers to Leadership Positions (03/30/2026)Lawsuit Claims Lyft Driver Sexually Assaulted Woman With Her Children in the Back Seat (03/26/2026)Uber Settlements Reached To Resolve Certain Sexual Assault Lawsuits (03/18/2026) Jury Selection Underway in First Bard PowerPort Trial Over Infection Claims (Posted: 4 days ago)The first Bard PowerPort lawsuit bellwether trial commences next week involving claims that a man suffered a severe infection due to the port catheter’s allegedly defective design.MORE ABOUT: BARD POWERPORT LAWSUITJudge Blocks Juries From Hearing About IVC Filter Problems in Bard PowerPort Trials (04/08/2026)Port-a-Cath Lawsuit Alleges Power P.A.C. 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