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.
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.
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.
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.
Sports Betting Addiction Lawsuit Sports betting addiction lawsuits are being investigated for college students and young adults who developed gambling problems after using apps like FanDuel and DraftKings, alleging that the platforms failed to warn about the addictive nature of their features and marketing practices.
Recalled Artificial Tears Caused Blindness in One Eye For Florida Firefighter: Lawsuit When tested, the recalled Artificial Tears used by the firefighter were found to contain large amounts of Pseudomonas Aeruginosa bacterial contamination. February 27, 2023 Russell Maas Add Your Comments A Florida fire department captain has filed a lawsuit against the manufacturers and distributors of recalled EzriCare Artificial Tears, claiming the contaminated eye drops caused him to develop an infection that resulted in complete vision loss in one eye. The complaint (PDF) was filed by Adam Disarro in the U.S. District Court Middle District of Florida on February 23, indicating that he suffers partial blindness and an uncertain future of medical complications as a result of a Pseudomonas Aeruginosa infection caused by recalled Artificial Tears, which have been linked to dozens of similar reports in recent months. The claim is one of growing number of Artificial Tears lawsuits filed in the wake of an EzriCare and Delsam Pharma eye drops recall first announced in early February, each involving similar claimms that the eye drops were marketed as safe, even though the manufacturers and distributors failed to perform proper microbial testing, which allowed contaminated eye drops to be distributed throughout the United States in recent months. Stay Up-to-Date About eye drop recalls AboutLawsuits.com sends a weekly digest email with information about recalls, lawsuits and warnings that may impact your family. "*" indicates required fields Email* SIGN ME UP Δ Learn More Stay Up-to-Date About eye drop recalls AboutLawsuits.com sends a weekly digest email with information about recalls, lawsuits and warnings that may impact your family. "*" indicates required fields Email* SIGN ME UP Δ Learn More Eye Drops Vision Loss Lawsuit Disarro indicates he purchased a two-pack of EzriCare Artificial Tears through Amazon.com on May 12, 2022, and again on September 12, 2022, and began using the eye drops almost immediately to assist with his dry eye condition. However, shortly after Disarro began using the EzriCare eye drops he began to experience irritation, swelling, extreme pain and discomfort in the eyes and skull, sensitivity to light and blurred vision. The pain ultimately caused him to seek emergency medical treatment at a Miami, Florida hospital where an eye specialist obtained cultures and confirmed his complications were the result of an active Pseudomonas Aeruginosa infection. After weeks of suffering, Disarro underwent light therapy in conjunction with a very aggressive treatment of fortified eye drops to beat the eye infection, however, Disarro was ultimately left with disfigurement and blindness to his left eye as a result of the recalled eye drops. The complaint states that three of the four bottles of Ezricare eye drops Disarro purchased through Amazon were tested at the Bascom-Palmer Eye Institute laboratory, which confirmed all three bottles contained a heavy growth of Pseudomonas Aeruginosa bacteria. Disarroโs lawsuit claims the manufacturers and distributors have a duty to ensure the Artificial Tears products are safe for human use, which the lawsuit claims they negligently failed to uphold. The complaint also claims the defendants engaged in deceptive and unfair business practices which led to Disarroโs injuries and damages, which include pain and suffering, mental anguish, emotional distress, physical impairment, physical disfigurement, loss of enjoyment of life, lost wages and lost earning capacity. Artificial Tears Eye Drop Recall Update The first Artificial Tears recall was announced by the U.S. Food and Drug Administration (FDA) on February 2, 2023, impacting 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 However, on February 22, the FDA recommended that a Delsam Pharma Artificial Eye Ointment recall be issued as well, and the manufacturer agreed just a day later. The FDAโs recommendation to recall Delsam Pharma Artificial Eye Ointment was made following a determination that the products may be contaminated with the same bacteria in Artificial Tears eye drops, which were not put through microbial testing to confirm they were bacteria-free. ย Lawyers Are Reviewing Artificial Tears Infection Lawsuits Nationwide At least a half dozenย Pseudomonas Aeruginosa infection lawsuitsย andย eye drops class action lawsuitsย have been filed on behalf of individuals exposed to the bacteria, and it is expected that the number of confirmed problems linked to the products will continue to grow significantly in the coming weeks and months. Lawyers are actively reviewing 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 Infection Partial Blindness Permanent Blindness Bloodstream Infection Other injuries caused by the eye drops Written by: Russell Maas Managing Editor & Senior Legal Journalist Russell 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 Recall, Blindness, Eye Drops, Eye Drops Recall, Eye Ointment Recall, EzriCare Eye Drops, 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 CommentsThis 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 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 Term Δ MORE TOP STORIES Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (Posted: 2 days ago) An Illinois woman has joined a growing number of plaintiffs alleging that the Medtronic Intellis neurostimulator, and similar devices, may fail to relieve chronic pain and instead lead to worsening complications. 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