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 Tampax Tampon Lawsuit Claims Feminine Hygiene Products Contain PFAS, Heavy Metals July 15, 2026 Colonoscopy Infection Lawsuit Filed Over Contaminated Olympus Scope July 14, 2026 SmartPort Catheter Lawsuit Claims Defective AngioDynamics Port-a-Cath Caused Infection July 14, 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. NameThis 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 Colonoscopy Infection Lawsuit Filed Over Contaminated Olympus Scope (Posted: yesterday)Olympus faces a lawsuit from a Chicago woman who says she developed a severe, life-threatening infection due to the design of its endoscopes, which she says can trap infectious material in their cracks and crevices.MORE ABOUT: SCOPE INFECTION LAWSUITOlympus Scope Infection Concerns Follow Years of FDA Warnings Over Reusable Endoscopes (07/02/2026)Olympus 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) Spinal Cord Stimulator Lawsuit Claims Boston Scientific Sales Reps Made Unauthorized Device Adjustments (Posted: 2 days ago)A Boston Scientific spinal cord stimulator lawsuit claims the chronic pain implants are defectively designed, causing a Louisiana woman to suffer shocks and pain, as well as dizziness and fainting spells.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro SCS Lawsuits Warrant Centralization in New MDL: Motion (07/08/2026)Proclaim Spinal Cord Stimulator Lawsuit Follows Infection, Battery Migration Problems (07/06/2026)MDL Sought for Abbott Spinal Cord Stimulator Lawsuits (06/29/2026) First Covidien Hernia Mesh Lawsuit Trial Over Symbotex Problems To Begin Next Week (Posted: 5 days ago)The first Covidien hernia mesh bellwether trial begins on Monday in Massachusetts federal court involving claims that the Symbotex mesh is defectively designed.MORE ABOUT: HERNIA MESH LAWSUITCovidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications (06/10/2026)Bard 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)
Colonoscopy Infection Lawsuit Filed Over Contaminated Olympus Scope (Posted: yesterday)Olympus faces a lawsuit from a Chicago woman who says she developed a severe, life-threatening infection due to the design of its endoscopes, which she says can trap infectious material in their cracks and crevices.MORE ABOUT: SCOPE INFECTION LAWSUITOlympus Scope Infection Concerns Follow Years of FDA Warnings Over Reusable Endoscopes (07/02/2026)Olympus 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)
Spinal Cord Stimulator Lawsuit Claims Boston Scientific Sales Reps Made Unauthorized Device Adjustments (Posted: 2 days ago)A Boston Scientific spinal cord stimulator lawsuit claims the chronic pain implants are defectively designed, causing a Louisiana woman to suffer shocks and pain, as well as dizziness and fainting spells.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro SCS Lawsuits Warrant Centralization in New MDL: Motion (07/08/2026)Proclaim Spinal Cord Stimulator Lawsuit Follows Infection, Battery Migration Problems (07/06/2026)MDL Sought for Abbott Spinal Cord Stimulator Lawsuits (06/29/2026)
First Covidien Hernia Mesh Lawsuit Trial Over Symbotex Problems To Begin Next Week (Posted: 5 days ago)The first Covidien hernia mesh bellwether trial begins on Monday in Massachusetts federal court involving claims that the Symbotex mesh is defectively designed.MORE ABOUT: HERNIA MESH LAWSUITCovidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications (06/10/2026)Bard 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)