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.
Recall Issued for 15 Million Surge Protectors After Injuries, Fire Risk October 4, 2013 Russell Maas Add Your CommentsA massive recall has been issued for nearly 15 million surge protectors after hundreds of reports involving the products over heating and causing smoke damage, which has resulted in over $1.5 million in property damage and at least 13 injuries from burns and smoke inhalation. ย The APC SurgeArrest surge protectors recall was announced by the U.S. Consumer Product Safety Commission (CPSC) on October 3, after the manufacturer received at least 700 reports of overheating surge protectors.Reports indicate 55 consumers experienced property damage in homes amounting in $916,000 and $750,000 in offices, as well as reports indicating consumers suffered from smoke inhalation and contact burns from touching the overheated surge protectors.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 recall includes APC 7 and 8 series Surge Arrest surge protectors manufactured before 2003 with the following model numbers; 7 series models with model numbers NET7, NET7T, NET7T-C, PER7, PER7C, PER7T, PER7T-CO, PER7TX137, PER7-U, PER7-U, PER7X148, PRF7T, PRO7, PRO7C, PRO7T, and PRO7TX183, and 8 series with model numbers NET8, NET8N, PER8T, PER8TR, PER8TR-CN, PER8TVR, PER8XTV, PRF8T2, PRF8TT, PRO8, PRO8T2, PRO8T2C, PRO8T2MP12, PRO8T2MP12B, PRO8TV. The affected surge protectors also have the words Personal, Professional, Performance, or Network printed on them.The products were manufactured in China under American Power Conversion (APC), currently known as Schneider Electric Corp., located in West Kingston, Rhode Island, where they were sold at Best Buy, Circuit City, CompUSA, and other stores nationwide from January 1993 through December 2002 for between $13 and $50.Consumers with affected products should cautiously unplug them and contact Schneider Electric at (888) 437-4007 or visit them online at http://recall.apc.com or www.apc.com and navigate to the โRecallโ link to submit a claim and receive more information on how to obtain a free replacement surge protector. 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: Fire, Surge Protector Recall Image Credit: |More Lawsuit Stories Bard PowerPort Fracture Lawsuit Set For Second Bellwether Trial in Aug. 2026 May 29, 2026 Spinal Cord Stimulator Malpractice Lawsuit Claims Device Left Veteran Partially Paralyzed May 29, 2026 Top Fitness Lawsuit Claims Home Gym Machine Failed, Crushing Womanโs Legs May 29, 2026 0 Comments EmailThis 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 Bard PowerPort Fracture Lawsuit Set For Second Bellwether Trial in Aug. 2026 (Posted: yesterday)The second Bard PowerPort bellwether trial is now scheduled to begin in August after the plaintiff in a claim originally planned for trial next month died, and her family stopped pursuing litigation.MORE ABOUT: BARD POWERPORT LAWSUITJury Returns Defense Verdict in First Bard PowerPort Injury Lawsuit (05/11/2026)Jury Selection Underway in First Bard PowerPort Trial Over Infection Claims (04/16/2026)Judge Blocks Juries From Hearing About IVC Filter Problems in Bard PowerPort Trials (04/08/2026) Dupixent Cancer Lawsuit Claims Eczema Drug Caused Womanโs CTCL Diagnosis (Posted: 2 days ago)A Delaware woman has filed a Dupixent lawsuit, claiming manufacturers promoted the eczema drug as a breakthrough treatment while failing to warn that it may trigger or worsen CTCL, a rare form of non-Hodgkinโs lymphoma.MORE ABOUT: DUPIXENT LAWSUITLink Between Dupixent and Cancer Withheld From Doctors and Users, Lawsuit Alleges (05/11/2026)Lawsuit Indicates Dupixent Lymphoma Diagnosis Resulted in Multiple Rounds of Chemotherapy (05/01/2026)Judges Will Consider MDL for Dupixent Cancer Lawsuits Late Next Month (04/21/2026) Omnipod Recall Impacts Another 7 Million Defective Pods That May Cause DKA, Hospitalization (Posted: 3 days ago)Federal regulators have expanded an Omnipod recall after reports that internal tubing defects may cause insulin leaks and under-delivery, potentially triggering dangerous blood sugar spikes.MORE ABOUT: OMNIPOD RECALL LAWSUITRecalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (04/30/2026)Insulet OmniPod 5 Recall Lawsuits May Be Filed Over Problems Resulting in Diabetic Ketoacidosis, Hospitalization and Death (03/24/2026)Omnipod 5 Insulin Pump Recall Follows Reports of Serious Injuries: FDA (03/20/2026)
Spinal Cord Stimulator Malpractice Lawsuit Claims Device Left Veteran Partially Paralyzed May 29, 2026
Bard PowerPort Fracture Lawsuit Set For Second Bellwether Trial in Aug. 2026 (Posted: yesterday)The second Bard PowerPort bellwether trial is now scheduled to begin in August after the plaintiff in a claim originally planned for trial next month died, and her family stopped pursuing litigation.MORE ABOUT: BARD POWERPORT LAWSUITJury Returns Defense Verdict in First Bard PowerPort Injury Lawsuit (05/11/2026)Jury Selection Underway in First Bard PowerPort Trial Over Infection Claims (04/16/2026)Judge Blocks Juries From Hearing About IVC Filter Problems in Bard PowerPort Trials (04/08/2026)
Dupixent Cancer Lawsuit Claims Eczema Drug Caused Womanโs CTCL Diagnosis (Posted: 2 days ago)A Delaware woman has filed a Dupixent lawsuit, claiming manufacturers promoted the eczema drug as a breakthrough treatment while failing to warn that it may trigger or worsen CTCL, a rare form of non-Hodgkinโs lymphoma.MORE ABOUT: DUPIXENT LAWSUITLink Between Dupixent and Cancer Withheld From Doctors and Users, Lawsuit Alleges (05/11/2026)Lawsuit Indicates Dupixent Lymphoma Diagnosis Resulted in Multiple Rounds of Chemotherapy (05/01/2026)Judges Will Consider MDL for Dupixent Cancer Lawsuits Late Next Month (04/21/2026)
Omnipod Recall Impacts Another 7 Million Defective Pods That May Cause DKA, Hospitalization (Posted: 3 days ago)Federal regulators have expanded an Omnipod recall after reports that internal tubing defects may cause insulin leaks and under-delivery, potentially triggering dangerous blood sugar spikes.MORE ABOUT: OMNIPOD RECALL LAWSUITRecalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (04/30/2026)Insulet OmniPod 5 Recall Lawsuits May Be Filed Over Problems Resulting in Diabetic Ketoacidosis, Hospitalization and Death (03/24/2026)Omnipod 5 Insulin Pump Recall Follows Reports of Serious Injuries: FDA (03/20/2026)