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.
Artificial Tears Infection Outbreak Has Impacted Nearly 70 People in 16 States, Per CDC Update The CDC is still investigating whether the Artificial Tears infection outbreak occurred due to contamination during the manufacturing process. March 15, 2023 Russell Maas Add Your Comments Following an initial Artificial Tears eye drops recall was announced in early February, federal health officials continue to discover additional individuals who suffered severe eye infections and other injuries caused by antibiotic-resistant bacteria that contaminated several different products distributed throughout the U.S. The U.S. Center for Disease Control and Prevention (CDC) released an Artificial Tears outbreak update on March 14, indicating that the agency is now aware of at least 68 individuals from 16 different states who used recalled eye drops and developed severe eye infections or blood stream infections, including individuals who required hospitalization and some who experienced total vision loss. This includes at least 12 new cases since the recall was first announced, leading health officials to reiterate warnings that consumers and medical providers should immediately stop using EzriCare and Delsam Pharma Artificial Tears eye drops, which have been found to be contaminated with carbapenem-resistant Pseudomonas aeruginosa in opened bottles. Artificial Tears Infection Recall Information about the Artificial Tears infection outbreak first surfaced in late January, 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 of Artificial Tears lawsuits brought both by individuals diagnosed with infections, as well as consumer class action claims that seek economic damages and medical monitoring. 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 The 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 include Delsam Pharma Artificial Eye Ointment as well. According to the latest CDC update, after cases were initially limited to 11 states, the agency now reports cases have spread across 16 states, with clear no geographic relevance to one another. 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 firsts began looking at the Artificial Tears products after several Pseudomonas aeruginosa outbreaks in nursing homes surfaced in Connecticut and Utah, and have indicated that elderly or infirmed individuals may face the greatest risk. 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 eye Eye pain or discomfort Redness of the eye or eyelid Feeling of something in your eye (foreign body sensation) Increased sensitivity to light Blurry vision At this time, the CDC is continuing to work with state agencies and announced that testing of unopened bottles of EzriCare Artificial Tears is ongoing to determine whether contamination may have occurred during manufacturing. Artificial Tears Eye Drops Lawsuits As the number of reported eye drops infections continue to rise, a series of eye drops lawsuits 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 claim that, as a result, consumers have now suffered eye infections that have resulted in permanent vision loss and other injuries. 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 Did You Experience an Artificial Tears Eye Infection? Lawsuits are being pursued for individuals who may be entitled to financial compensation after experience eye infections from contaminated Artificial Tears. FIND OUT IF YOU QUALIFY Tags: Artificial Tears, Blindness, Eye Infection, Eye Injury, EzriCare Eye Drops, Infection, 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 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 TermEmailThis 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)