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.
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 CommentsNameThis 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 Depo-Provera Meningioma Warning Update Should Be Added to Birth Control Shot: Lawsuit (Posted: today)A Depo-Provera meningioma lawsuit argues that Pfizer had a duty to warn women about scientific evidence linking the birth control shot to potential brain tumor growth yet failed to do so.MORE ABOUT: DEPO-PROVERA LAWSUITHearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (04/15/2026)High-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (04/06/2026)Depo-Provera Meningioma Lawyers Reappointed to MDL Leadership Roles (03/25/2026) Judges Will Consider MDL for Dupixent Cancer Lawsuits Late Next Month (Posted: yesterday)A group of federal judges will determine whether all Dupixent cancer lawsuits should be formed into a multidistrict litigation, following oral arguments set for May 28.MORE ABOUT: DUPIXENT LAWSUITDupixent Injections Caused Peripheral T-Cell Lymphoma (PTCL) Diagnosis: Lawsuit (04/06/2026)Link Between Dupixent and CTCL Withheld From Users, Medical Community: Lawsuit (03/31/2026)Drug Makers Agree Dupixent Cancer Lawsuits Should Be Centralized in MDL (03/26/2026) SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation (Posted: 2 days ago)A product liability lawsuit alleges unlicensed Abbott representatives made real-time spinal cord stimulator programming decisions based on a Texas womanโs responses, improperly modifying the device and contributing to her injuries.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITWaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (04/14/2026)Boston Scientific Neuromodulation Lawsuit Claims Spinal Cord Stimulator Exacerbated Chronic Pain (04/08/2026)Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (04/03/2026)
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 Warning Update Should Be Added to Birth Control Shot: Lawsuit (Posted: today)A Depo-Provera meningioma lawsuit argues that Pfizer had a duty to warn women about scientific evidence linking the birth control shot to potential brain tumor growth yet failed to do so.MORE ABOUT: DEPO-PROVERA LAWSUITHearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (04/15/2026)High-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (04/06/2026)Depo-Provera Meningioma Lawyers Reappointed to MDL Leadership Roles (03/25/2026)
Judges Will Consider MDL for Dupixent Cancer Lawsuits Late Next Month (Posted: yesterday)A group of federal judges will determine whether all Dupixent cancer lawsuits should be formed into a multidistrict litigation, following oral arguments set for May 28.MORE ABOUT: DUPIXENT LAWSUITDupixent Injections Caused Peripheral T-Cell Lymphoma (PTCL) Diagnosis: Lawsuit (04/06/2026)Link Between Dupixent and CTCL Withheld From Users, Medical Community: Lawsuit (03/31/2026)Drug Makers Agree Dupixent Cancer Lawsuits Should Be Centralized in MDL (03/26/2026)
SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation (Posted: 2 days ago)A product liability lawsuit alleges unlicensed Abbott representatives made real-time spinal cord stimulator programming decisions based on a Texas womanโs responses, improperly modifying the device and contributing to her injuries.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITWaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (04/14/2026)Boston Scientific Neuromodulation Lawsuit Claims Spinal Cord Stimulator Exacerbated Chronic Pain (04/08/2026)Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (04/03/2026)