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.
Lawsuit Alleges Infection From Recalled Eye Drops Caused Permanent Vision Damage, Light SensitivityThe antibiotic-resistant strain of bacteria found in recalled Artificial Tears eye drops can lead to inflammation and destruction of eye tissue, resulting in irreversible blindness, according to allegations raised in the complaint. July 8, 2024 Irvin Jackson Add Your CommentsA product liability lawsuit filed by a California woman claims she has been left with potentially irreversible vision damage after using Ezricare Artificial Tears eye drops, which were recalled shortly after she purchased them through Amazon.com, following reports of similar infections linked to bacterial contamination.The complaint (PDF) was brought by Shannon Urioste in the U.S. District Court for the District of New Jersey on June 26, pursuing damages from the manufacturers of the recalled eye drops, including Ezricare LLC, EzrRx LLC and Global Pharma Healthcare Private Ltd.The eye drops were part of a massiveย Artificial Tears recallย first announced by the U.S. Food and Drug Administration (FDA) in February 2023, following at least 55 reports involving users who sufferedย eye infections after exposure to bacteria in the eye drops.The strain ofย Pseudomonas aeruginosaย linked to recalled eye drops poses a major health risk, due to its antibiotic resistance and capability of mutating quickly. In severe cases, Pseudomonas aeruginosa may cause endophthalmitis, which is a rare but serious infection of the eyeball that can cause inflammation and destruction of the tissue throughout the eye, resulting in irreversible blindness.Urioste now joins a growing number of consumers who are pursuing Artificial Tears eye drop vision damage lawsuits, alleging that bacteria in the bottles caused a wide range of health problems, including vision loss, eye infections, bloodstream infections and other injuries. At leastย four deaths have now been linked to the eye drops, and a number of other users required surgical removal of their eye due to infections from the recalled Artificial Tears.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 lawsuit indicates Urioste, of San Bernadino, purchased two bottles of Ezricare Artificial Tears eye drops in early January 2023 through Amazon.com. A little more than a month later, the eye drops were recalled.However, Urioste had already used them, and began to suffer redness, irritation and swelling in both eyes. It was only when she visited her doctor that Urioste became aware that the eye drops had been recalled due to infection risks.According to the complaint, Urioste was diagnosed with acute bacterial conjunctivitis in both eyes.โAs a result of Ms. Uriosteโs use of EzriCare Artificial Tears and the subsequent infection she was diagnosed with, Ms. Urioste suffered from injury to both her eyes and to her vision,โ the lawsuit indicates. โHer eyes are potentially permanently affected by the infection, as she now suffers from light sensitivity, constant dryness, burning, and itching, and she also sees spots within her field of vision.โShe presents claims of failure to warn, design and manufacturing defect, negligence, gross negligence, negligent misrepresentation/omission, fraud, fraudulent concealment, breach of warranty, negligent failure to timely recall, and violation of New Jersey consumer protection laws. Urioste seeks both compensatory and punitive damages. 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: Amazon, Artificial Tears, Bacterial Contamination, Eye Drops, Eye Drops Recall, Ezricare, EzriCare Eye Drops, Infection, Vision LossMore Eye Drops Recall Lawsuit Stories 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 Target Eye Drops Lawsuit Filed Over Bacterial Contamination that Led to Vision Loss January 22, 2024 0 CommentsInstagramThis 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 Judge Sets Next Covidien Hernia Mesh Lawsuit for Trial in January 2027 (Posted: yesterday)The U.S. District Judge presiding over all Covidien hernia mesh lawsuits has scheduled the next bellwether trial to begin on January 11.MORE ABOUT: HERNIA MESH LAWSUITCovidien Mesh Lawyers to Meet With MDL Judge This Week, Following Landmark Verdict (08/17/2026)Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (08/05/2026)Hernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026) Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit (Posted: 2 days ago)A South Carolina woman alleges an Abbott spinal cord stimulator malfunction caused painful electrical shocks that required removal surgery less than two years after implantation.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (09/04/2026)Judge Allows Back Stimulator Lawsuits Against Boston Scientific to Be Directly Filed in MDL (08/31/2026)Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (08/26/2026) Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (Posted: 3 days ago)The second Bard PowerPort lawsuit bellwether trial has ended in a $40 million verdict for the plaintiff who had the implant removed after the catheter broke and traveled to her heart.MORE ABOUT: BARD POWERPORT LAWSUITNearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026)Bard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)New Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026)
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