Hintermann Ankle Replacement Problems Draw New FDA Warning Over โHigher-Than-Expectedโ Failure Rates
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.
HDX and PowerMate Air Compressor Recall Issued Due to Shock Hazard February 13, 2014 Russell Maas Add Your CommentsRoughly 107,000 HDX and PowerMate electric air compressors sold primarily at Home Depot and Menardโs stores have been recalled, after the manufacturer recognized the potential for the terminalsย of the pressure switch to contact the motor housing, which may pose a serious shock hazard for consumers. ย The air compressor recall was announced by the U.S. Consumer Product Safety Commission (CPSC) on February 12, impacting products sold under the brand names HDX and PowerMate. The compressors feature a potentially dangerous design defect, which may cause consumers to suffer a shock injury if the terminals of the pressure switch come into contact with the motor housing.The recall includes two gallon HDX air compressors with model numbers VSP0000201.HDX, VSP0000201.HDX1 and SKU number 947282. These air compressors are gray and have HDX printed on a white label located on the top cylinder. Also included in the recall are two gallon Powermate air compressors with model numbers VSP0000201.01, VSP000020.KIT and VSP0000201.NS. These products are red with โPowermateโ printed in white on the top cylinder.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 COMPENSATIONBoth brands of recalled air compressors are 120-volt powered, with a maximum operating pressure of 100 PSI and air delivery of .4 SCFM at 90 PSI. The compressors are both designed to have two, one gallon air tanks stacked upon one another.The affected air compressors were manufactured in China under MAT Industries LLC of Long Grove, Illinois where they were sold at Home Depot, Menards, and other hardware stores nationwide, as well as online at Homedepot.com from June 2010 through October 2013 for between $80 and $120.The CPSC recommends that consumers stop using the affected air compressors immediately and contact MAT Industries at 855-992-2300 or visit them online at either www.powermate.com or www.homedepot.com for free repairs. 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: Air Compressor Recall, Electrocution Image Credit: |More Lawsuit Stories Failed Cartiva Implant Required Multiple Toe Surgeries, Lawsuit Alleges June 11, 2026 Hintermann Ankle Replacement Problems Draw New FDA Warning Over โHigher-Than-Expectedโ Failure Rates June 11, 2026 Little Giant Articulating Ladder Lawsuit Alleges Collapse Resulted in Hip, Elbow Fractures June 11, 2026 1 Comments Andrea June 7, 2023 I have this compressor and didn’t know it was recalled. I was looking for a part for it when I found out it was recalled. Who should I contact, Home Depot? 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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 Covidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications (Posted: yesterday)A Covidien hernia mesh lawsuit will go before a jury next month after a federal judge rejected the manufacturer’s motion to have the case dismissed.MORE ABOUT: HERNIA MESH LAWSUITBard Ventralight Lawsuit Claims Hernia Mesh Failure Resulted in Ongoing Physical Disabilities (06/03/2026)Bard Ventralex Patch Lawsuit Claims Umbilical Hernia Mesh Failed, Requiring Removal Surgery (05/21/2026)Covidien ProGrip Mesh Complications Lawsuit Filed Over Alleged Defects and Failure To Warn Patients (04/21/2026) Olympus Endoscope Lawsuit Filed Over ERCP Infection, Sepsis Linked to Contaminated Scope (Posted: 2 days ago)Lawsuit alleges Olympus failed to address known problems with sterilizing duodenoscopes, leading to a fatal ERCP infection years after federal regulators first raised concerns about the devices.MORE ABOUT: SCOPE INFECTION LAWSUITPediatric 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) Boston Scientific Stimulator Lawsuits Centralized in Federal MDL (Posted: 3 days ago)Federal regulators have centralized at least 23 Boston Scientific spinal cord stimulator lawsuits in a multidistrict litigation that excludes multiple similar claims involving Abbott and Nevro implants.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (06/02/2026)Spinal Cord Stimulator Malpractice Lawsuit Claims Device Left Veteran Partially Paralyzed (05/29/2026)Abbott Spinal Cord Stimulator Problems Resulted in Severe Paralysis: Lawsuit (05/19/2026)
Hintermann Ankle Replacement Problems Draw New FDA Warning Over โHigher-Than-Expectedโ Failure Rates June 11, 2026
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