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.
Home Depot Table Saws Recalled Due to Laceration Hazard December 15, 2010 Staff Writers Add Your CommentsAbout 21,500 Ryobi portable table saws, sold exclusively at Home Depot, have been recalled due design defects that may result in a laceration risk for individuals using the table saw or those standing nearby.ย The Home Depot table saw recall was announced on Tuesday by the U.S. Consumer Product Safety Commission (CPSC), after the manufacturer received a report from a consumer who was hit by a piece of metal that flew out of the machine while cutting.The CPSC has determined that the saw blade on the motor carriage could be misaligned. Although there have been no reported injuries or property damages in connection with the defective portable table saws, this could pose a serious hazard for consumers.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 affects about 21,500 Ryobi RTS20 portable table-saws, which have a blue base and warning label on the rear of the saw with Ryobi and the model number RTS20 printed on it.The saws were sold at Home Depots in the United States and Canada from July 2010 through October 2010 for about $200. They were distributed by One World Technologies, of Anderson, South Carolina and were made in China.This is the second Ryobi recall in less than two months. In mid-October, the CPSC announced a recall of 455,000 Ryobi Model HP 1802M cordless power drills after the company received 47 reports of overheating, 12 of which resulted in fires that caused property damage to homes and vehicles and minor injuries. The drills were also sold exclusively at Home Depot.Any consumers who own one of the recalled table saws should contact Ryobi for a free inspection and free repair or replacement if necessary. For more information, consumers can contact Ryobi at 1-800-597-9624 or visit the companyโs website at www.ryobitools.com. Tags: Home Depot, Ryobi, Table SawMore Table Saw Lawsuit Stories FTC Seeks To Scrap SawStop Requirements for Table Saws September 23, 2025 Table Saw Safety Regulations In Limbo For Foreseeable Future August 31, 2017 Table Saw Settlement Results in $2M Payment for Middle Finger Amputation May 30, 2017 1 Comments Benjamin May 9, 2017 what am i supposed to do with the Ryobi RTS20 table saw that i have ? am i supposed to take it back to home depot? i have no receipt now.. its been a since july/aug 2010… NO one answers the recall line.. i was on line hold for 21 min.. i hung up. not happy CompanyThis 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 Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (Posted: today)An AngioDynamics Vortex port lawsuit alleges the implantable port catheter caused a South Carolina woman to suffer pulmonary embolisms and a serious infection requiring surgical removal.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITAngioDynamics Port Catheter Lawsuit Claims Womanโs SmartPort Implants Caused Multiple Infections (06/23/2026)Xcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis (06/12/2026)Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (06/03/2026) Proclaim Spinal Cord Stimulator Lawsuit Follows Infection, Battery Migration (Posted: yesterday)A Texas man’s lawsuit claims the electrodes and battery of an Abbott spinal cord stimulator tried to push out of his skin, resulting in a severe infection and the need for surgical removal.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITMDL Sought for Abbott Spinal Cord Stimulator Lawsuits (06/29/2026)Lawsuit Alleges WaveWriter Alpha Spinal Cord Stimulator Problems Caused Burning, Shocking Sensations (06/24/2026)Abbott Spinal Cord Stimulator Battery Problems Led to Repeat Surgeries, Lawsuit Claims (06/16/2026) Olympus Scope Infection Concerns Follow Years of FDA Warnings Over Reusable Endoscopes (Posted: 5 days ago)Federal warnings and enforcement actions involving Olympus and other reusable medical scopes have raised concerns that design flaws may allow bacteria to remain trapped after cleaning, leading to serious infections and product liability lawsuits.MORE ABOUT: SCOPE INFECTION LAWSUITOlympus Endoscope Lawsuit Filed Over ERCP Infection, Sepsis Linked to Contaminated Scope (06/09/2026)Pediatric Sepsis Cases Contribute to More Than 1,800 Childrenโs Deaths Annually in U.S.: Study (03/31/2026)Infections After Colonoscopy, ERCP May Result in Lawsuits Over Olympus Scope Problems (03/27/2026)
Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (Posted: today)An AngioDynamics Vortex port lawsuit alleges the implantable port catheter caused a South Carolina woman to suffer pulmonary embolisms and a serious infection requiring surgical removal.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITAngioDynamics Port Catheter Lawsuit Claims Womanโs SmartPort Implants Caused Multiple Infections (06/23/2026)Xcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis (06/12/2026)Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (06/03/2026)
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