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.
ReliOn Insulin Syringe Recall: Sold at Wal-Mart and Sam’s Club November 6, 2008 AboutLawsuits Add Your CommentsNearly half a million ReliOn Insulin Syringes sold at Walmart stores and Sam’s Clubs throughout the United States have been recalled because some of the syringes could contain up to 2.5 times the appropriate dose. This could pose a substantial risk of a serious and potentially fatal insulin overdose.ย The ReliOn Insulin Syringe recall applies to only one lot of syringes labeled as “ReliOn 1cc, 31-gauge syringes, 100 units for use with U-100 insulin”. The affected Lot Number is 813900.The hypodermic syringes are single-use, disposable and sterile, with permanently affixed needles. They were distributed by the manufacturer to Wal-marts and Sam’s Clubs throughout the United States between August 1, 2008 and October 8, 2008.ย The FDA posted a notice on their website yesterday notifying healthcare providers and consumers about the insulin syringe recall. The manufacturer, Tyco Healthcare Group LP (Covidien) has received at least one report of an adverse reaction caused by use of one of the defective syringes.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 COMPENSATIONReceiving an insulin syringe with more than the indicated dose, could lead to a risk of an insulin overdose, possibly resulting in hypoglycemia (low blood sugar levels) or even death. Symptoms of an insulin overdose could include anxiety, confusion, extreme hunger, irritability, sweating, tremors or trembling hands, increased pulse rate, irregular heart beat, headaches or nausea.The FDA recall notice indicates that an undisclosed number of syringes intended for use with U-40 insulin were mixed with syringes intended for use with U-100 insulin. Although the syringes are packaged individually, they were then sold in boxes labeled as 100 units for use with U-100 insulin.Tyco indicates that only one lot is impacted by the manufacturing problems with the insulin syringes. However, there were 471,000 syringes distributed as part of this lot, which were sold in 4,710 boxes.All of the insulin syringes were manufactured by Tyco Healthcare Group LP, distributed Can-Am Care Corp and sold exclusively at Wal-Mart stores and Sam’s Clubs under the ReliOn Insulin Syringe brand name.Walmart has sent letters to over 16,500 customers notifying them of the insulin syringe recall, and the FDA has asked all consumers and healthcare providers to carefully check any insulin syringes they have to make sure they are not impacted by this recall.Recalled syringes can be returned to any Sam’s Club Pharmacy or local Wal-Mart store. However, lawyers who are investigating potential ReliOn Insulin Syringe recall lawsuits have recommended that any individuals who believe they may have suffered an adverse reaction caused by the defective syringes, should hold onto any remaining syringes if they intend to pursue legal action.Any unused insulin syringes which are not returned to the store so that they can be preserved for lawsuit purposes, should be stored in a manner to prevent unintended future use of the product. Tags: Insulin, ReliOn Insulin Syringe, Sterile Syringe, Syringe, Tyco, WalmartMore Lawsuit Stories SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation April 20, 2026 Lawsuits Over Cartiva Real-World Failure Rates Continue To Roll Into MDL April 20, 2026 Barton Pressure Cooker Lawsuit Claims Explosion Resulted in Third- and Fourth-Degree Burns April 20, 2026 1 Comments Louella January 23, 2024 I suffered a staph infection from Religion pen Needles in September 2023, which I had to have surgery for and are still having side affects. And have bad scars on my body plus burning in my stomach. 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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 SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation (Posted: today)A product liability lawsuit alleges unlicensed Abbott representatives made real-time spinal cord stimulator programming decisions based on a Texas womanโs responses, improperly modifying the device and contributing to her injuries.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITWaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (04/14/2026)Boston Scientific Neuromodulation Lawsuit Claims Spinal Cord Stimulator Exacerbated Chronic Pain (04/08/2026)Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (04/03/2026) Passenger in Uber Sexual Assault Trial Tells Jury She Feared Driver Knowing Her Address (Posted: 3 days ago)The second federal Uber sexual assault bellwether trial is underway in North Carolina, involving claims a woman was groped and had to flee from the driver.MORE ABOUT: UBER SEXUAL ASSAULT LAWSUITMDL Judge Appoints Lyft Sexual Assault Lawyers to Leadership Positions (03/30/2026)Lawsuit Claims Lyft Driver Sexually Assaulted Woman With Her Children in the Back Seat (03/26/2026)Uber Settlements Reached To Resolve Certain Sexual Assault Lawsuits (03/18/2026) Jury Selection Underway in First Bard PowerPort Trial Over Infection Claims (Posted: 4 days ago)The first Bard PowerPort lawsuit bellwether trial commences next week involving claims that a man suffered a severe infection due to the port catheter’s allegedly defective design.MORE ABOUT: BARD POWERPORT LAWSUITJudge Blocks Juries From Hearing About IVC Filter Problems in Bard PowerPort Trials (04/08/2026)Port-a-Cath Lawsuit Alleges Power P.A.C. Break Down Resulted in Serious Port Catheter Infection (03/31/2026)Final Pretrial Conference in Bard PowerPort Lawsuit To Be Held April 9 (03/27/2026)
SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation April 20, 2026
Barton Pressure Cooker Lawsuit Claims Explosion Resulted in Third- and Fourth-Degree Burns April 20, 2026
SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation (Posted: today)A product liability lawsuit alleges unlicensed Abbott representatives made real-time spinal cord stimulator programming decisions based on a Texas womanโs responses, improperly modifying the device and contributing to her injuries.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITWaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (04/14/2026)Boston Scientific Neuromodulation Lawsuit Claims Spinal Cord Stimulator Exacerbated Chronic Pain (04/08/2026)Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (04/03/2026)
Passenger in Uber Sexual Assault Trial Tells Jury She Feared Driver Knowing Her Address (Posted: 3 days ago)The second federal Uber sexual assault bellwether trial is underway in North Carolina, involving claims a woman was groped and had to flee from the driver.MORE ABOUT: UBER SEXUAL ASSAULT LAWSUITMDL Judge Appoints Lyft Sexual Assault Lawyers to Leadership Positions (03/30/2026)Lawsuit Claims Lyft Driver Sexually Assaulted Woman With Her Children in the Back Seat (03/26/2026)Uber Settlements Reached To Resolve Certain Sexual Assault Lawsuits (03/18/2026)
Jury Selection Underway in First Bard PowerPort Trial Over Infection Claims (Posted: 4 days ago)The first Bard PowerPort lawsuit bellwether trial commences next week involving claims that a man suffered a severe infection due to the port catheter’s allegedly defective design.MORE ABOUT: BARD POWERPORT LAWSUITJudge Blocks Juries From Hearing About IVC Filter Problems in Bard PowerPort Trials (04/08/2026)Port-a-Cath Lawsuit Alleges Power P.A.C. Break Down Resulted in Serious Port Catheter Infection (03/31/2026)Final Pretrial Conference in Bard PowerPort Lawsuit To Be Held April 9 (03/27/2026)