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.
Freeze Off Wart Removers Linked to Burn, Fire Risk: FDA Warns January 21, 2014 Martha Garcia Add Your CommentsFederal health officials are warning consumers about the potential risk of fires and severe burns from freeze off wart removers, also known as cryogenic wart removers.The FDA issued a warn remover warning last week, indicating that over-the-counter (OTC) cryogenic wart removers have been linked to more than a dozen injury reports. However, no specific brand name products were identified in connection with the burns.Dr. Schollโs Freeze Away Wart Remover, Compound W Freeze Off, and Wartner Cryogenic Wart Removal System are among widely used brands of over-the-counter products that contain a mixture of liquid dimethyl ether and propane, which are highly flammable substances.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 COMPENSATIONCryogenic products work by freezing warts from the skin. However, at least 14 people have reported to federal health officials that they experienced burns, singed hair or skin redness after using the products.According to the FDA warning, the canisters caught fire in some cases during use, injuring consumers and causing property damage in several instances. At least three patients reported a candle nearby contributed to the incidents, but 11 of the reports found no ignition source was involved. In the reports, the dispenser typically caught fire when the mixture was released from its pressurized canister.“This is extremely concerning, especially because people may not be aware that everyday household items like curling irons and straight irons can be hot enough to be an ignition source for these products,” said Karen Nast, RN and FDA Nurse Consultant, in the FDA statement.Wart Removers Considered Medical DevicesThe FDA has regulated wart removers as a medical device since 2009. The products come with specific use instructions because of the high level of flammability and the types of chemicals involved.Consumers are instructed to saturate an applicator with the mixture, which is cooled to -40 degrees Celsius. They should then press the applicator to the wart for a specified amount of time.Warts are growths caused by the human papilloma virus (HPV) infection. An average of three to four applications are required for full effectiveness. Calloused skin may take more treatments.Warts may often disappear on their own without a cryogenic treatment, but may take some time.ย The FDA advises consumers to contact health care professionals to determine if a cryogenic treatment is necessary.Professional treatments may include, surgical paring, laser or liquid nitrogen cryosurgical treatments. This offers consumers wart treatments performed by a trained medical professional in a safe office setting.Other OTC treatments which may also be alternatives to the cryogenic treatment include topical applications of salicylic acid. This will soften the skin and loosen warts so they fall off or can be easily removed.Health officials recommend consumers use the products only as directed. Consumers are cautioned to use it in a well-ventilated area, away from flames or other heat sources.Consumers should also take care to carefully dispose of empty containers, if punctured or exposed to heat they may explode and cause severe injuries.The report warns these types of events are often under reported to the correct authorities. The FDA encourages consumers to report all types of events and injuries. 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: Fire, Wart RemoverMore Lawsuit Stories Lawsuit Alleges Suboxone Dental Damage Warnings Were Issued Too Late May 7, 2026 Lyft Passenger Lawsuit Alleges Rideshare Company Never Responded to Sexual Assault Claim May 7, 2026 Misha Knee System Lawsuit Alleges Defective Implant Required Second Surgery May 7, 2026 0 Comments NameThis 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 Suboxone Dental Damage Warnings Were Issued Too Late (Posted: today)The makers of Suboxone continue to face lawsuits claiming that use of the opioid treatment film strips can cause severe dental damage.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITStudy Finds No Birth Defect Risks From Suboxone When Compared to Methadone (04/30/2026)Judge Says Suboxone โSchedule Aโ Lawsuits Should Be Filed Individually or Dismissed (04/27/2026)Court Outlines Plan To Prepare Suboxone Tooth Decay Lawsuits for Trial in Early 2028 (04/02/2026) Nevro Stimulator Lawsuit Alleges SCS Lead Failure Caused Nerve Damage (Posted: 2 days ago)A spinal cord stimulator lawsuit filed against Nevro Corporation claims two of its implants have failed in a man’s back, leaving him with nerve damage and increasing pain.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (04/29/2026)JPML Sets Hearing Over Spinal Cord Stimulator Lawsuit Consolidation for May 28 (04/24/2026)SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation (04/20/2026) Galaflex Breast Mesh Lawsuits Filed Against Becton Dickinson in Rhode Island (Posted: 2 days ago)Women nationwide have begun filing GalaFLEX breast mesh lawsuits against BD, claiming they suffered pain, permanent injuries and the need for revision surgery after the implants were used off-label for breast reconstruction.MORE ABOUT: BREAST MESH LAWSUITBreast Mesh Implant Complications Often Leave Women Asking If They Have a Lawsuit (03/05/2026)Cosmetic Surgeons Warn Against Using Internal Bra Mesh for Breast Lifts (12/11/2025)GalaFLEX Breast Mesh Problems Were Highlighted in Warnings Issued by Former Becton Dickinson Medical Director (11/14/2025)
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