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.
Siemens Circuit Breaker Recall Issued Due to Fire Hazard September 24, 2010 Staff Writers Add Your Comments About 2.2 million Siemens and Murray circuit breakers have been recalled due to a defective spring clip that can cause it to arc and potentially catch fire.ย The circuit breaker recall was announced on Thursday by the U.S. Consumer Product Safety Commission (CPSC) after Siemens Industry Inc., the manufacturer, received a report that a spring clip in the circuit breaker had broken during installation. The defective circuit boards could be a fire hazard. A broken spring clip can lead to a loss of force to maintain a proper electrical connection in the panelboard, according to the CPSC. If the electrical connection is not constant, there could be excessive heat, arcing or thermal damage at the connection point which could damage the panelboardโs insulation, resulting fire, damage and possibly injury. Do You Know about… Spinal Cord Stimulator lawsuits Spinal 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 More SEE IF YOU QUALIFY FOR COMPENSATION Do You Know Aboutโฆ Spinal Cord Stimulator lawsuits Spinal 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 More SEE IF YOU QUALIFY FOR COMPENSATION The recall affects 2.2 million Siemens and Murray 15 through 50 AMP single and double pole circuit breakers, load centers and meter combos. The load centers are circuit breakers that include an electrical panel, and the meter combos are a load center and a meter socket. All of the recalled products are labeled โSiemensโ or โMurrayโ and have a date code of 0610 or 0710 and the catalog number printed on a label on the side of the circuit breakers. The load centers and meter combos have date codes between June 23, 2010 and August 25, 2010 stamped on the inside of the metal box. A complete list of the catalog numbers affected is listed on the recall announcement. The recalled circuit breakers were sold at The Home Depot, Lowes, hardware stores, building supply stores and electrical distributers nationwide between June 2010 and August 2010 for between $2.50 and $235. The CPSC recommends that any consumers who possess or have installed the recalled circuit breakers contact Siemens for a free inspection and a free replacement product. The firmโs website is www.usa.siemens.com. Tags: Fire, Home Depot, Product Recall More Lawsuit Stories 10 Hair Relaxer Lawsuits Selected by Court for Early Trial Dates April 7, 2026 Lawsuit Claims Roblox Showed Reckless Disregard for Child Safety April 7, 2026 Kenmore Dehumidifier Lawsuit Alleges Device Ignited, Caused More Than $150,000 in Damages April 7, 2026 4 Comments Dan June 7, 2012 I have a 100 amp Siemens load center manufacture date 11 feb 08. The main breaker appears to be bad. one side was loosing power frequently flipped the breaker off and on again and power was back up. Decided to replace the main breaker and I am feeling unsure about the other breakers in the panel at this point. Has anyone complained about this with a panel that pre-dates the 2010 recall??? WOODY February 12, 2011 MURRAY, CROUSE HINDES, ITE, ARROW HART….ALL ARE BYTHE SAME PARENT CORP…..ALL ARE JUNK !! Charles January 10, 2011 I have emailed Siemens twice about this issue and they do not respond with any information on how to get it replaced. Do they wait for a fire and then offer to replace the breaker? What do you have to do to get Siemens to respond? Daniel September 30, 2010 Hello, I do have some breaker with 0610 and i also installed some during the last few monts. I would like more info. on the recall. If i go back on my jobs to inspect or change breakers, will i be reinbursed by siemens or Eddy’s buiding supply LinkedInThis 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 No Post Comment I authorize the above comments be posted on this page Weekly 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 Term Δ MORE TOP STORIES 10 Hair Relaxer Lawsuits Selected by Court for Early Trial Dates (Posted: yesterday) A federal judge has selected 10 hair relaxer lawsuits to serve as potential bellwether trials after altering the selection process to eliminate non-representative cases. MORE ABOUT: HAIR RELAXER LAWSUITHair Relaxer Class Action Lawsuit Seeks Certification for Medical Monitoring Claims (04/01/2026)Hair Relaxer Endometrial Cancer Lawsuits and Ovarian Cancer Lawsuits Proposed for Early Trials (03/23/2026)Lawyers To Nominate Hair Relaxer Cancer Cases for Early Bellwether Trials Next Week (03/12/2026) High-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (Posted: 2 days ago) A Depo-Provera lawsuit indicates that a Washington state woman must receive ongoing medical monitoring and brain scans due to a high-risk brain tumor allegedly caused by the birth control shot. MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Meningioma Lawyers Reappointed to MDL Leadership Roles (03/25/2026)Depo-Provera Brain Tumor Symptoms Reported Among Birth Control Users (03/19/2026)Depo Injection Lawsuit Claims Birth Control Shot Caused Meningioma Brain Tumor (03/17/2026) Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (Posted: 5 days ago) An Illinois woman has joined a growing number of plaintiffs alleging that the Medtronic Intellis neurostimulator, and similar devices, may fail to relieve chronic pain and instead lead to worsening complications. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Spinal Cord Stimulator Lawsuits Filed Over Device Malfunction, Failure (03/30/2026)Abbott Proclaim SCS Lawsuit Alleges Stimulator Lead Migration Resulted in Multiple Surgeries (03/24/2026)Abbott, Boston Scientific Oppose Spinal Cord Stimulator Lawsuit MDL (03/20/2026)
Kenmore Dehumidifier Lawsuit Alleges Device Ignited, Caused More Than $150,000 in Damages April 7, 2026
10 Hair Relaxer Lawsuits Selected by Court for Early Trial Dates (Posted: yesterday) A federal judge has selected 10 hair relaxer lawsuits to serve as potential bellwether trials after altering the selection process to eliminate non-representative cases. MORE ABOUT: HAIR RELAXER LAWSUITHair Relaxer Class Action Lawsuit Seeks Certification for Medical Monitoring Claims (04/01/2026)Hair Relaxer Endometrial Cancer Lawsuits and Ovarian Cancer Lawsuits Proposed for Early Trials (03/23/2026)Lawyers To Nominate Hair Relaxer Cancer Cases for Early Bellwether Trials Next Week (03/12/2026)
High-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (Posted: 2 days ago) A Depo-Provera lawsuit indicates that a Washington state woman must receive ongoing medical monitoring and brain scans due to a high-risk brain tumor allegedly caused by the birth control shot. MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Meningioma Lawyers Reappointed to MDL Leadership Roles (03/25/2026)Depo-Provera Brain Tumor Symptoms Reported Among Birth Control Users (03/19/2026)Depo Injection Lawsuit Claims Birth Control Shot Caused Meningioma Brain Tumor (03/17/2026)
Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (Posted: 5 days ago) An Illinois woman has joined a growing number of plaintiffs alleging that the Medtronic Intellis neurostimulator, and similar devices, may fail to relieve chronic pain and instead lead to worsening complications. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Spinal Cord Stimulator Lawsuits Filed Over Device Malfunction, Failure (03/30/2026)Abbott Proclaim SCS Lawsuit Alleges Stimulator Lead Migration Resulted in Multiple Surgeries (03/24/2026)Abbott, Boston Scientific Oppose Spinal Cord Stimulator Lawsuit MDL (03/20/2026)