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.
Saniderm Hand Sanitizer Recall Issued Following Three Deaths And Report Of Blindness June 30, 2020 Russell Maas Add Your CommentsFollowing three deaths and at least one report involving problems that resulted in blindness, federal health officials have announced a recall of Saniderm hand sanitizer products distributed for sale on the East Coast, due to potentially toxic ingredients.The FDA announced the hand sanitizer recall on June 27, after the manufacturer acknowledged the hand sanitizers were produced with methanol, a wood alcohol that may result in serious and life threatening injuries if consumed.According to health officials, Saniderm hand sanitizer products have been linked to at least three deaths after consumers attempted to drink the products, which is an unfortunate misuse of hand sanitizers among some with alcohol problems. There was also at least one reported case in which the hand sanitizer resulted in blindness in Mexico.Do You Know about…Spinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONDo You Know AboutโฆSpinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONOfficials are warning that the active ingredient in the hand sanitizer, methanol, can cause nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system or death if accidentally or intentionally consumed, raising concerns about misuse or children who may get access to the bottles.The recall includes Saniderm Advanced Hand Sanitizer 1-liter plastic bottles with an orange twist-top cap that are marked with the lot number 53131626. The products were manufactured in Mexico by Eskbiochem SA de CV on April 1, 2020 and were distributed for sale in the United States to retailers in Virginia, Maryland and New Jersey on April 15, 2020.Hand sanitizers are intended to be used when soap and water are not available. However, they have become increasingly popular in the home and office settings. The topical antiseptics typically containing between 40% and 90% ethyl alcohol are left on the hands and not rinsed off with water.While millions of Americans use hand sanitizers daily, sometimes multiple times a day, to reduce bacteria, growing concerns have also emerged amid thousands of reports annually of hand sanitizer poisonings to U.S. Poison Control Centers, often involving young children.The American Association of Poison Control Centers (AAPCC) reports roughly 9,300 incidents of hand sanitizer poisonings were recorded in the first half of 2017, and more than 12,000 were recorded in the first half of 2018. The agency further reported more than 70,000 reports of hand sanitizer poisoning among children were recorded by the U.S. Centers for Disease Control and Prevention (CDC) from 2011 to 2014, involving both alcohol based and non-alcohol based hand sanitizers.Hand sanitizer products often come in bright colors, with scents similar to food and candy, including some that contain glitter or fun characters in the bottles, which make the products especially appealing to young children.While a child is able to lick or ingest a small amount of hand sanitizer from their hands without becoming sick, if they swallow even a dime-sized amount, they will most likely experience alcohol poisoning that could result in confusion, vomiting, and drowsiness. In severe cases, they may suffer respiratory arrest, or even death.While FDA-approved hand sanitizers all pose a risk to consumers who accidentally ingest them, the newly recalled products containing methanol pose a severe risk of injury or death if accidentally or intentionally ingested.Although methanol poisoning typically only last eight to 24 hours, the severity of the injuries that can arise from the accumulation of acid in the blood, called metabolic acidosis, can set in fast and cause permanent blindness or death.Officials are urging consumers to immediately quarantine any of the recalled products and to put them out of reach of children or those who may potentially consume the hand sanitizer.Consumers with questions regarding this voluntary recall can contact Saniderm at +1 (415) 562-5502 orย info@sanidermproducts.com Written by: Russell MaasManaging Editor & Senior Legal JournalistRussell 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: Hand Sanitizer, Hand Sanitizer Recall, Methanol, Poison, SanidermMore Lawsuit Stories Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect June 12, 2026 Xcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis June 12, 2026 Rezurock Lawsuit Claims GVHD Medication Caused Debilitating Skin Condition, Prurigo Nodularis June 12, 2026 1 Comments Bridget August 3, 2021 Walgreens selling for 25 cents I bought a ton saying it was on shelves too long due to Covid FacebookThis 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 Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (Posted: yesterday)A spinal cord stimulator lawsuit claims that the Abbott Proclaim XR 5 system failed to treat a manโs chronic pain, instead leaving him with shocks and burning sensations.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026)Lawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (06/02/2026)Spinal Cord Stimulator Malpractice Lawsuit Claims Device Left Veteran Partially Paralyzed (05/29/2026) Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (Posted: 2 days ago)A Suboxone dental erosion lawsuit filed by nine plaintiffs accuses the manufacturer of knowing the film strips caused severe tooth decay and other oral health problems, but failed to warn the medical community or patients.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (05/20/2026)Lawsuit Alleges Suboxone Dental Damage Warnings Were Issued Too Late (05/07/2026)Study Finds No Birth Defect Risks From Suboxone When Compared to Methadone (04/30/2026) Covidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications (Posted: 3 days ago)A Covidien hernia mesh lawsuit will go before a jury next month after a federal judge rejected the manufacturer’s motion to have the case dismissed.MORE ABOUT: HERNIA MESH LAWSUITBard Ventralight Lawsuit Claims Hernia Mesh Failure Resulted in Ongoing Physical Disabilities (06/03/2026)Bard Ventralex Patch Lawsuit Claims Umbilical Hernia Mesh Failed, Requiring Removal Surgery (05/21/2026)Covidien ProGrip Mesh Complications Lawsuit Filed Over Alleged Defects and Failure To Warn Patients (04/21/2026)
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Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (Posted: yesterday)A spinal cord stimulator lawsuit claims that the Abbott Proclaim XR 5 system failed to treat a manโs chronic pain, instead leaving him with shocks and burning sensations.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026)Lawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (06/02/2026)Spinal Cord Stimulator Malpractice Lawsuit Claims Device Left Veteran Partially Paralyzed (05/29/2026)
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