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.
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.
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.
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
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.
Change Healthcare Lawsuit Lawyers are reviewing Change Healthcare class action lawsuits for individuals who had their personal information stolen due to the data breach.
AngioDynamics Port Catheter 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.
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.
Processed Food Lawsuit Lawsuits are being pursued against the food industry over their manufacturing and advertising of ultra-processed foods, which have caused a generation of children to face an increased risk of developing childhood diabetes and other chronic illnesses.
AFFF Lawsuit Exposure to firefighting foam chemicals may result in an increased risk of cancer for firefighters, military and airport personnel.
Lawsuit Alleges Recalled Artificial Tears Eye Drops Caused Vision Loss Plaintiff used recalled Artificial Tears eye drops for at least 45 days, leading to potentially permanent eye damage and vision loss. March 30, 2023 Irvin Jackson Add Your Comments A Minnesota man has filed a lawsuit over vision loss caused by recalled Artificial Tears eye drops, indicating that an antibiotic resistant strain of Pseudomonas aeruginos bacteria in bottles distributed throughout the United States has left him with permanent eye damage. Riley Kerkhoff filed the complaint (PDF) in the U.S. District Court for the District of New Jersey on March 22, naming Ezricare LLC, EZRIRX LLC, Global Pharma Healthcare Private LTD, and Amazon.Com, Inc. as the defendants. The claim is one of growing number of eye drops lawsuits filed in the wake of an EzriCare and Delsam Pharma Artificial Tears recall first announced in early February, each involving similar claims that users developed severe infections caused by bacterial contamination that was not discovered until after the bottles were sold to unsuspecting consumers. EYE DROPS RECALL LAWSUITS Did you or a loved one use recalled eye drops? Lawyers are investigating EzriCare Artificial Tears lawsuits for individuals who experienced eye infections, blindness or other problems following use of the recalled eye drops. Learn More SEE IF YOU QUALIFY FOR COMPENSATION EYE DROPS RECALL LAWSUITS Did you or a loved one use recalled eye drops? Lawyers are investigating EzriCare Artificial Tears lawsuits for individuals who experienced eye infections, blindness or other problems following use of the recalled eye drops. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Kerkhoff indicates he purchased two bottles of Artificial Tears online through Amazon.com in November 2022. He used the eye drops for about 45 days before he started to notice swelling, redness and discharge from his eyes. According to the complaint, Kerkhoff went to the emergency room and was diagnosed with a bacterial infection, which was treated with antibiotics. However, the infection continued to progress and he states that he indicates the recalled Artificial Tears eye drops caused vision loss, which may be permanent. The lawsuit alleges Ezricare and other defendants failed to properly ensure the Artificial Tears eye drops were safe for consumer use, leading to catastrophic injuries. “Defendants knew that the risk of exposure to Pseudomonas Aeruginosa bacteria from use of its products was not readily recognizable to an ordinary consumer and that consumers would not inspect the product for bacteria,” the lawsuit states. “Defendants did not adequately test and/or give adequate warnings to Plaintiff that the EzriCare Artificial Tears were contaminated with the Pseudomonas Aaeruginosa bacteria or about the dangers of the presence of Pseudomonas Aeruginosa bacteria in their artificial tear products.” Recalled Artificial Tears Eye Infections The recalled Artificial Tears eye drops have been found to contain Carbapenem-Resistant Pseudomonas Aeruginosa (CRPA), which is bacteria that may result in infections resulting in mild to severe health consequences, including fever, chills, body aches, light-headedness, rapid pulse, heavy breathing, nausea and vomiting, diarrhea and decreased urination. However, the strain of Pseudomonas aeruginosa linked to the Artificial Tears recall 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. According to a recent update on the Artificial Tears infection outbreak issued by the U.S. Centers for Disease Control and Prevention (CDC), the agency is aware of at least 68 cases of recalled Artificial Tears eye infections in 16 states, including three deaths, eight reports of vision loss and four reports of infections which resulted in eye removal surgery. Eye Drop Infection Lawsuits As new information continues to be released about the history of the eye drops infection outbreak, it is expected that the number of Pseudomonas aeruginosa infection lawsuits over the recalled eye drops will increase in the coming weeks and months. Lawyers are actively investigating potential eye drop infection lawsuits against the manufacturers and distributors of EzriCare and Delsam Pharma’s eye drops for multiple injuries and side effects caused by the contamination, including; Eye Infection Partial Blindness Permanent Blindness Bloodstream Infection Other injuries caused by the eye drops Review a Lawsuit Over Recalled Artificial Tears Eye Drops Lawyers provide free consultations and claim evaluations to help users determine whether they may be entitled to settlement benefits for vision loss and other eye damage caused by recalled Artificial Tears eye drops. FIND OUT IF YOU ARE ELIGIBLE Tags: Artificial Tears, Eye Drops Recall, Eye Infection, Eye Injury, EzriCare Eye Drops, Infection, Vision Loss 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 Comments 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 No Post Comment I authorize the above comments be posted on this page Weekly 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 TermPhoneThis field is for validation purposes and should be left unchanged. Δ MORE TOP STORIES New Bard Hernia Mesh Lawsuits Continue To Be Filed Following Global Settlement (Posted: today) In the six months since a Bard hernia mesh settlement agreement was reached, at least two dozen new lawsuits have been brought, as the implants continue to fail and require revision surgery. 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Lawsuit Alleges Infection From Recalled Eye Drops Caused Permanent Vision Damage, Light Sensitivity July 8, 2024
Amazon Artificial Tears Lawsuit Filed Over Bacterial Keratitis Infection from Contaminated Eye Drops February 15, 2024
New Bard Hernia Mesh Lawsuits Continue To Be Filed Following Global Settlement (Posted: today) In the six months since a Bard hernia mesh settlement agreement was reached, at least two dozen new lawsuits have been brought, as the implants continue to fail and require revision surgery. MORE ABOUT: HERNIA MESH LAWSUITHernia Surgery Malpractice Lawsuit Cleared To Move Forward Over Botched Procedure (03/21/2025)Mediation To Discuss Settling Covidien Hernia Mesh Lawsuits Set for March 31 Through April 4 (03/14/2025)Covidien Hernia Mesh Settlement Talks To Get Underway After Parties Select Mediator Next Week (02/19/2025)
Four BioZorb Breast Tissue Marker Lawsuits Selected for Bellwether Trials (Posted: yesterday) As new BioZorb lawsuits continue to be filed over complications with the recalled breast tissue markers, lawyers indicate they are on track for the first of four test cases to go before a jury in September 2025. MORE ABOUT: BIOZORB LAWSUITCourt Clears BioZorb Lawsuit Design Defect Claims Over Recalled Breast Tissue Marker (03/26/2025)Group of 7 BioZorb Injury Lawyers Appointed to Leadership Positions in Lawsuits Over Recalled Breast Tissue Marker (03/19/2025)Breast Cancer Survivors File Lawsuit Over Recalled BioZorb Tissue Marker (03/12/2025)
Depo-Provera Meningioma Diagnosis Information Required To Qualify for Lawsuit: Order (Posted: 2 days ago) Women pursuing Depo-Provera meningioma lawsuits will have to provide documentary proof of their diagnosis and the versions of the birth control shot they received within 120 days of filing their case. MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Lawsuit Timeline for Preparing Pilot Trial Cases Outlined by MDL Judge (03/24/2025)Women Can File Depo-Provera Brain Tumor Lawsuits Directly in MDL: Court Order (03/18/2025)75 Lawyers in Depo-Provera Lawsuits Seek MDL Leadership Roles (03/10/2025)