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.
Artificial Tears Eye Drops Infection Outbreak First Detected in Connecticut Nursing Home: APInvestigators found that contaminated eye drops caused several nursing home eye infection outbreaks last year, months before a nationwide Artificial Tears recall was announced March 1, 2023 Russell Maas Add Your CommentsAs officials continue to track a growing eye drops infection outbreak, which has already resulted in a recall for certain EzriCare and Delsam Pharma Artificial Tears products, a new report details how initial cases of the infection quickly spread throughout several nursing homes.While concerns about bacterial contamination in Artificial Tears products have only been publicly known for about a month, health officials say they have been tracking infection case reports since May 2022, involving individuals hospitalized with antibiotic resistant strains of Pseudomonas Aeruginosa in California.According to a news report by the Associated Press, the first eye drops bacterial infection case was reported at an ophthalmologist office in Los Angeles County, when a patient was seen for symptoms of a severe eye infection. The office quickly identified the cause of the infection to be a rare form of Pseudomonas Aeruginosa containing genes that protected it from common antibiotics.After the ophthalmologist’s office performed advanced genetic testing, they quickly identified the severity of the bacterial infection at hand, and reported the case to the U.S. Centers for Disease Control and Prevention (CDC). The same eye doctorโs office would go on to treat two additional cases of the infection in the coming months.Unbeknownst the eye doctorโs office, they had reported the first case of what would become a nationwide Artificial Tears eye drops infection outbreak. But the extent of the problems would not be discovered until a cluster of eye infections at Connecticut nursing homes were identified weeks later.Eye Drops Infection Outbreak Surfaced June 2022In June 2022, several outbreaks of Pseudomonas Aeruginosa infection were reported to the Connecticut health department after five nursing homes experienced antibiotic resistant outbreaks, sickening a total of 25 patients. It was then that health experts began to recognize there was a problem, which has since expanded to result in a nationwide eye drops recall and a number of Artificial Tears eye infection lawsuits now being pursued against manufacturers of certain contaminated products.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 MoreOnly a few months after the Connecticut infections were identified, officials from Davis County, Utah also reported six cases of the antibiotic resistant infections to the CDC in August 2022.By early November, CDC officials had ruled out the possibility the bacterial contamination was caused by any local piece of equipment at the individual facilities and began to narrow down the root cause of the outbreak to a product. On November 9, CDC investigators made a breakthrough when they determined each of the facilities reporting outbreaks in Florida, Connecticut and Utah reported administering EzriCare Artificial Tears to patients prior to infection onset.The first public warnings about the Artificial Tears eye drops infection outbreak were released in late January 2023, when the CDC was able to confirm through genetic sequencing that the infections reported after using EzriCare products in Florida, Utah and Connecticut were in fact caused by the same strain of Pseudomonas Aeruginosa.EzriCare Artificial Tears RecallFollowing the CDCโs discoveries, the U.S. Food and Drug Administration (FDA) issued theย Artificial Tears eye drops recallย on February 2, warning customers to stop using the products immediately as the CDC continues the investigate a growing outbreak of Pseudomonas Aeruginosa infections among users of certain EzriCare and Delsam Pharma Artificial Tears products.The recall now includes Artificial Tears products sold through Amazon.com and Walmart under the brand names EzriCare, as well as Delsam, with the following UPC and NDC codes;Ezricare (blue box): NDC 79503-0101-15 with UPC 3 79503 10115 7, andDelsam Pharma (white box): NDC 72570-121-15 with UPC -72570-0121-15As a of February 21, 2023, the CDCโs investigation into Artificial Tears Pseudomonas aeruginosa eye infections has identified 58 illnesses across 13 states. The CDC is currently aware of 35 patient illnesses occurring in healthcare facility outbreaks, which has resulted in one death and at least five individuals suffering vision loss.Eye Drop Infection LawsuitsAs new information continues to be released about the history of the eye drops infection outbreak, it is expected that the number ofย Pseudomonas aeruginosa infection lawsuits over the recalled eye drops will increase in the coming weeks and months.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: 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: Artificial Tears, Connecticut, Eye Drops, Eye Drops Recall, Eye Infection, EzriCare Eye Drops, Infection, Nursing Home, Vision Loss Image Credit: |More 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 CommentsCommentsThis 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 Boston Scientific Spectra WaveWriter Lawsuit Alleges Lead Fracture, Migration and Painful Electric Shocks (Posted: today)A woman’s Boston Scientific Spectra WaveWriter SCS lawsuit claims improper hermetic seals lead to short circuits, failures.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Spinal Cord Stimulator Lead Problems Caused Burning, Shocks, Lawsuit Alleges (10/16/2026)Master 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) Dupixent Skin Cancer Lawsuit Filed After Man Diagnosed With Mycosis Fungoides (Posted: yesterday)A man’s Dupixent skin cancer lawsuit claims the eczema treatment led to a CTCL diagnosis.MORE ABOUT: DUPIXENT LAWSUITDupixent Cancer Risks Lead Experts to Recommend Skin Biopsies Before Treatment (10/16/2026)Dupixent Lawyers Seek Leadership Positions in MDL Over Cancer Risks (10/01/2026)Dupixent Side Effects Lawsuit Alleges Drug Caused Cutaneous T-Cell Lymphoma (09/24/2026) Fujifilm and Olympus Scope Infection Risks Highlight Growing Need for Advanced Disinfection Systems: Report (Posted: 2 days ago)Concerns about life-threatening infections associated with reusable medical scopes are increasing the need for advanced disinfection technology to protect patients from bacterial contamination.MORE ABOUT: SCOPE INFECTION LAWSUITOlympus Medical Device Warning Letter Follows FDA Inspections of Six Manufacturing Facilities (10/16/2026)Olympus Scope Wrongful Death Lawsuit Filed Over ERCP Infection (09/03/2026)Olympus Colonoscopy Lawsuit Over C. 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