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.
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
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.
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.
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.
Personal Emergency Response Kit Recalled Due to Remote Battery Failure September 12, 2013 Russell Maas Add Your CommentsA recall has been issued for Visonic personal emergency response system kits, following complaints that indicate that the warning signal for a low or dead battery may fail, posing a potential risk that the device will not work in life-threatening situations when users are in need assistance. ย The Visonic Amber Classic and Amber Select X Personal Response System kits recall was announced by the U.S. Consumer Product Safety Commission (CPSC) on September 11, following at least one report of the device failing to send a warning signal to the user and system administrator to replace the battery.Personal emergency response systems (PERS) are commonly used by the elderly, those who live alone, or people with health conditions that can be life threatening if not attended to immediately. The devices typically include a remote pendant that is worn or carried and a base station connected to a phone line within the home. This allows the person in need of help to press a button on the pendant that will send a signal to the base station alerting that assistance is needed.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 COMPENSATIONThe recalled Visonic Personal Response System Kits include the Amber Classic models with catalog number 0-7425 and serial numbers ranging between 0408044281 and 4410052723 and the Amber SelectX models with catalog number 0-100729 and serial numbers ranging between 2308600299 and 3013079617. The systems consists of white base stations that measure 9 inches wide by 7 inches deep and 2 inches high and have an emergency button that is red on the Classic model and grey on the SelectX model.The emergency system kits were manufactured in Israel by Visonic Ltd., of Tel Aviv, Israel where they were imported to the U.S. a sold at Visonic distributors and professional alarm installation firms nationwide from January 2008 through August 2013 for between $220 and $240 per kit.The CPSC recommends that those with affected emergency kits contact their system installer or Visonic at 800-223-0020 immediately to either reset the unit or add an additional base unit. Visonic is advising users not to try and reconfigure the device themselves and to manually test the Amber PERS pendant regularly for low battery alarms. 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: Battery, Battery Recall Image Credit: |More Lawsuit Stories Olympus Scope Wrongful Death Lawsuit Filed Over ERCP Infection September 3, 2026 Kalshi Sports Betting Lawsuit Alleges Prediction Market Violates Connecticut Gambling Laws September 3, 2026 Chlorpyrifos Pesticide Exposure May Promote Cardiovascular Injury: Study September 3, 2026 0 Comments CommentsThis 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 Olympus Scope Wrongful Death Lawsuit Filed Over ERCP Infection (Posted: today)A Kentucky man says his wife died of sepsis and infection complications linked to an Olympus endoscope used during an ERCP procedure.MORE ABOUT: SCOPE INFECTION LAWSUITOlympus Colonoscopy Lawsuit Over C. 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