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.
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
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.
Paraquat Parkinson’s Disease Lawsuits Exposure to the toxic herbicide Paraquat has been linked to a risk of Parkinson's disease.
Artificial Tears Eye Drops Infection Outbreak First Detected in Connecticut Nursing Home: AP Investigators 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 Comments As 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 doctor’s office would go on to treat two additional cases of the infection in the coming months. Unbeknownst the eye doctor’s 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 2022 In 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. 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 Only 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 Recall Following the CDC’s discoveries, the U.S. Food and Drug Administration (FDA) issued the Artificial Tears eye drops recall 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, and Delsam Pharma (white box): NDC 72570-121-15 with UPC -72570-0121-15 As a of February 21, 2023, the CDC’s 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 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 EzriCare Artificial Tears Infection Outbreak Lawsuits Were you or a loved one impacted by the Delsam Pharma and EzriCare Artificial Tears recall? Eye drops infection lawsuits are being reviewed for individuals who have experienced problems. FIND OUT IF YOU QUALIFY 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 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 TermNameThis field is for validation purposes and should be left unchanged. Δ MORE TOP STORIES Depo-Provera Meningioma Diagnosis Information Required To Qualify for Lawsuit: Order (Posted: today) 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) Cartiva SCI Lawsuit Alleges Toe Implant Worsened Pain, Decreased Range of Motion (Posted: yesterday) An Indiana woman has filed a Cartiva SCI implant lawsuit, indicating that the toe implant failed due to a defective design, resulting in the need for revision surgery and recommendations to permanently fuse her big toe. 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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
Depo-Provera Meningioma Diagnosis Information Required To Qualify for Lawsuit: Order (Posted: today) 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)
Cartiva SCI Lawsuit Alleges Toe Implant Worsened Pain, Decreased Range of Motion (Posted: yesterday) An Indiana woman has filed a Cartiva SCI implant lawsuit, indicating that the toe implant failed due to a defective design, resulting in the need for revision surgery and recommendations to permanently fuse her big toe. MORE ABOUT: CARTIVA IMPLANT LAWSUITCartiva Implant Injury Lawsuit Set for Trial in February 2026 (03/07/2025)Lawsuit Indicates Cartiva Implant Fails in 2 Out of 3 Patients, But Continued To Be Sold in U.S. (02/13/2025)Cartiva Toe Implant Lawsuit Filed Over Worsened Pain, Reduced Range of Motion and Need for Surgical Removal (02/07/2025)
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