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.
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
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.
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.
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.
Walmart and CVS Eye Ointment Recall Issued Over Infection RisksThe recall of Walmart and CVS eye ointments that pose an infection risk comes about a year after a massive Artificial Tears recall was linked to reports of severe eye injuries, vision loss and deaths. February 28, 2024 Hannah Brown Add Your CommentsLubricant eye ointment products sold by major retailers, including Walmart and CVS, have been recalled due to a risk that they could cause infections and vision loss.The U.S. Food and Drug Administration (FDA) announced the lubricant eye ointment recall on February 22, after discovering a potential lack of sterility in the products.The recall comes after a routine inspection by the FDA of the manufacturing facility, where they observed a lack of sterility assurance. Failure to ensure sterility in eye ointment products can potentially pose an increased risk to consumers, because the ointments bypass the bodyโs natural defenses when applied to the eyes.Eye Drop Contamination RisksThe findings come amid increased concerns about the sterility and safety of various eye care products, following a massive Artificial Tears recall announced in February 2023, due to the presence of Pseudomonas aeruginosa; a bacterial contaminant that is resistant to antibiotics, and can cause serious eye infections that can lead to irreversible blindness, death and the need for surgical eye removal.Since that recall, consumers have been warned about more than two dozen different over-the-counter eye drop products sold under several known brand names, including CVS, Target, and Rite Aid. According to a recent report by the U.S. Centers for Disease Control and Prevention (CDC), the recalled Artificial Tears eye drops have been linked to 81 cases of bacterial contamination, including multiple reports of vision loss, four reports of consumers requiring removal of an eyeball, and four reports of deaths.The contamination problems have led to a number of Artificial Tears lawsuits, alleging that bacteria in the eye drops caused a wide range of health problems. However, no infection incidents or Pseudomonas aeruginosa contamination have been linked to these latest recalled CVS and Walmart eye ointment 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 MoreLubricant Eye Ointment RecallThis latest recall impacts 25 lots of eye ointment products produced for Brassica Pharma Pvt. Ltd., which were then supplied to several distributors and sold under different brand names, including Equate Lubricant Eye Ointment, Equate Style Lubricant Eye Ointment, CVS Health Lubricant Eye Ointment, and Lubricant PM Ointment. Equate is Walmartโs in-house generic brand.The affected products were sold in 3.5 gram tubes in a cardboard box nationwide through distributors such as Walmart, CVA, and AACE Pharmaceuticals Inc. They carried expiration dates ranging from February 2024 to September 2025. A full list of affected products and UPC codes are listed in the recall notice linked above.To avoid a risk of serious eye injury, consumers are being warned to immediately stop use of the recalled eye ointment and return the products to the place of purchase. The FDA and the manufacturers are calling for distributors to immediately stop sale of these products and to return them to their distributors.Those with questions regarding this recall can contact Brassica Pharma Pvt. Ltd. at +1 833-225-9564 orย info@brassicapharma.com. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.Consumers and healthcare professionals are urged to report any adverse events linked to the recalled eye ointment products to the FDAโs MedWatch Adverse Event Reporting program. Tags: Artificial Tears, CVS, Eye Infection, Eye Ointment Recall, Infection, Vision Loss, WalmartMore 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 Nevro Stimulator Lawsuit MDL Request Opposed by Manufacturer (Posted: today)The JPML has been asked to reject a petition by plaintiffs seeking to consolidate all federal Nevro spinal cord stimulator lawsuits before one federal judge, claiming the injuries and claims are too different from plaintiff to plaintiff.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims (08/10/2026)Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (08/06/2026)Spine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026) Gulf War Veteran Parkinsonโs Disease Lawsuits Investigated Over Pesticide Use During Operations Desert Shield and Desert Storm (Posted: yesterday)Lawyers are investigating Parkinsonโs disease lawsuits for Gulf War veterans potentially exposed to the pesticide chlorpyrifos during Operations Desert Shield and Desert Storm.MORE ABOUT: CHLORPYRIFOS PARKINSONโS DISEASE LAWSUITAgricultural Workers Face Higher Risk of ALS Due to Pesticide Exposure: Study (08/10/2026)Paraquat Exposure Lawsuit Claims Farm Herbicide Caused Parkinsonโs Disease (08/06/2026)Chlorpyrifos Pesticide Side Effects Research Highlights Decades of Parkinsonโs Disease Risks (08/04/2026) Nearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (Posted: 2 days ago)C.R. 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Nearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (Posted: 2 days ago)C.R. Bard and its Becton Dickinson parent company face more than 3,700 Bard PowerPort lawsuits that claim the port catheters are defectively designed.MORE ABOUT: BARD POWERPORT LAWSUITBard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)New Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026)Bard PowerPort Fracture Lawsuit Set For Second Bellwether Trial in Aug. 2026 (05/29/2026)