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.
Companies Receive FDA Warning Letters Over False Ebola Treatment Claims September 25, 2014 Martha Garcia Add Your CommentsFederal drug regulators indicate that several companies are attempting to dupe consumers striken with fear over the possibility of an ebola pandemic spreading out of West Africa, illegally marketing ebola treatments and cures in the United States.ย The FDA issued warning letters to Natural Solutions Foundation, doTERRA International LLC, and Young Living, indicating that the companies are breaking the law by making misleading claims about potential treatments and cures for ebola.The Ebola epidemic in West Africa has killed nearly 3,000 people since it began earlier this year. The U.S. Centers for Disease Control and Prevention (CDC) says that the ebola outbreak could infect 500,000 people by the end of January.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 COMPENSATIONSeveral Americans have been brought back to the U.S. seeking treatment from the devastating illness, raising some concerns that the outbreak may take root in the U.S. However, many health officials say that is unlikely, given the strength of the U.S. water, sanitation and emergency response systems.Several companies have attempted to capitalize on the mounting ebola concerns, marketing products that claim to treat or cure the virus. However, no such products are approved as safe and effective by federal drug regulators.Unsubstantiated ClaimsNew Jersey based Natural Solutions was issued a warning letter after promoting their product, Nano Silver, as a cure for the disease.In messages written on the company’s websites, the organization claims that a Department of Defense funded a study in 2009 revealed โNano Silver inhibits the ebola virus.โ It also blatantly calls Nano Silver a โcure for ebola,โ and indicates that it is the โdefinitive prevention and therapy for ebola virus,โ and will help โalleviate the terrible pain of the disease.โThe FDA letter warns the company that it is illegal to make such claims without actually having “competent and reliable” scientific evidence to back it, as well as approval from the FDA. The agency says the company has none of those things.Utah-based doTERRA was also issued a warning letter concerning the line of Essential Oil products including scents like, Oregano, Frankincense, Geranium, Lavender, Peppermint, and others.The FDA says the oils are promoted as treatments for certain condition. The company marketed many of the products as treatments for viral infections, including ebola, bacterial infections, cancer, brain injury, autism, Alzheimerโs Disease, tumor reduction and other conditions.The companys’ website advertises the products with the marketing, โFight your virus with essential oils.โ It states oregano oil is โeffective in activating non-enveloped murine norovirus within 1 hour of exposure,โ and to treat โEbola virusโ as well.Young Living essential oils company, based out of Utah, was also issued a letter earlier this week. The FDA warns the company against marketing any essential oil products for unapproved FDA applications.The FDA found claims concerning the products on the company’s consultantโs websites. They included the claim, โViruses (including Ebola) are no match for Young Living Essential Oilsโ and the claim that the oil product โThievesโ is โhighly anti-microbial. . . It could help against Ebola.The FDA has also found the claims widely used across social networking sites, including Twitter and Facebook.The agency has requested the companies respond to the warning letters informing the FDA of corrective actions the company plans to take to correct the violations noted. The warning also indicates failure to implement โlasting corrective actionโ may result in regulatory action being initiated.The FDA and the Financial Industry Regulatory Authority (FINRA) issued warnings to health care professionals and consumers in August that opportunists were trying to take advantage of Ebola fears. The agencies warned companies and consumers about increasing reports of Ebola treatments and cures which have not been documented or FDA approved.Many of the fraudulent Ebola treatments are being sold online and in other marketplaces. Additionally, reports of scammers promoting stocks in companies that claim to have Ebola prevention products have also been received by the FINRA.The Ebola virus is believed to have started in Guinea in March and spread to Liberia, Sierra Leon and Nigeria. The virus has no known cure, however several Americans were infected and treated with an experimental vaccine and are making a full recovery. Written by: Martha GarciaHealth & Medical Research WriterMartha Garcia is a health and medical research writer at AboutLawsuits.com with over 15 years of experience covering peer-reviewed studies and emerging public health risks. She previously led content strategy at The Blogsmith and contributes original reporting on drug safety, medical research, and health trends impacting consumers. Tags: Dietary Supplement, Ebola, FINRA, FraudMore 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 0 Comments X/TwitterThis 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: 2 days ago)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: 3 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: 5 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)
Rezurock Lawsuit Claims GVHD Medication Caused Debilitating Skin Condition, Prurigo Nodularis June 12, 2026
Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (Posted: 2 days ago)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: 3 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: 5 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)