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.
Aspirin Alone Led to More Dangerous Blood Clots in Knee and Hip Replacement PatientsKnee and hip replacement patients often have high risk of blood clots in the days immediately after surgery August 24, 2022 Russell Maas Add Your CommentsA new study has found taking aspirin alone after a major joint replacement surgery may significantly increase the risk of developing blood clots.In findings published in the Journal of American Medical Association (JAMA) on August 23, researchers revealed that after a hip replacement or knee replacement surgery, patients given a prescription anticoagulants had a lower risk of developing symptomatic venous thromboembolism (VTE), when compared to treating with aspirin alone.As the number of total hip arthroplasty (THA) or total knee arthroplasty (TNA) procedures increase each year, more patients face risks of developing blood clots. During a joint replacement procedure, tissue, fat, or proteins can be released into the blood stream, causing the blood to thicken around these particles, creating a potential blockage. Patients may also experience blood clotting risks if veins are damaged during total knee or hip replacement surgeries.It is well known that total hip and knee replacement patients have the highest rate of developing blood clots within 10 days after surgery. However, depending on the patientsโ medical history, these blood clotting risks can remain high for up to three months following the surgery.Learn More AboutKnee Replacement LawsuitsIf you or a loved one experienced complications or required revision surgery due to a defective knee replacement implant, you may be entitled to financial compensation.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONLearn More AboutKnee Replacement LawsuitsIf you or a loved one experienced complications or required revision surgery due to a defective knee replacement implant, you may be entitled to financial compensation.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONIn this new study, researchers examined the rate of symptomatic VTE among 9,711 patients who underwent total hip and knee replacement across 31 Australian hospitals between April 20, 2019, and December 18, 2020. Of the participants, 5,675 were treated solely with aspirin following the surgery, while 4,036 were given only enoxaparin, which is a prescription anticoagulant most popularly sold under the brand name Lovenox. The rate of symptomatic VTE was then evaluated among both groups after 90 days post-surgery.According to the findings, symptomatic VTE occurred in 256 patients, including 79 cases of pulmonary embolism, 18 cases of above-knee deep vein thrombosis, and 174 cases of below-knee deep vein thrombosis.When comparing the two treatment groups, those being treated with Aspirin alone after THA or TNA were nearly twice as likely to develop symptomatic VTE as those taking enoxaparin within the first 90 days after surgery. The aspirin group was calculated at 3.45% and in the enoxaparin group was 1.82%.Researchers say the study offers insight as to how treating physicians can mitigate the risk of post joint replacement blood clotting events, which can result in serious and life threatening injuries to patients if the clot breaks away and reaches the lungs.Aspirin Bleeding Event ProblemsTreatment with aspirin as an over-the-counter blood thinner to reduce the risk of certain medical conditions such as heart attack, stroke and blood clots have been called into question by several recent medical studies.While aspirin was previously recommended as a daily preventative measure for many years for those who have known cardiovascular disease such as clogged heart arteries or history of heart attack or stroke, new guidelines suggest adults aged 70 and up should stop taking daily aspirin due to the risk of suffering severe internal bleeding.For those without cardiovascular disease, a daily aspirin regimen may not prevent injury, and could even increase the likelihood of an adverse health event, according to a July 2021 study published in the medical journalย JAMA Network Open.In April 2021, a study was published in JAMA Internal Medicine suggested that taking aspirin increases serious bleeding problems and hospitalization when used in combination with blood thinners like Xarelto or Eliquis together, while providing no meaningful benefits for users.Researchers concluded that aspirin did not appear to provide any clear benefits to account for the increased bleeding risks and hospitalizations, and emphasizes a need for doctors to change what they recommend to patients and help provide patient education about the risks of adding aspirin with anticoagulant medications.In another study published by the New England Journal of Medicine on October 8, researchers revealed that when given a combination of Plavix and aspirin, patients faced nearly twice the rate of bleeding events than exclusive treatments. 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: Aspirin, Blood Clots, Hip Replacement, Knee ReplacementMore Knee Replacement Lawsuit Stories Exactech Implant Settlement Results in $8M Payout Over High Failure Rates September 19, 2025 Settlement Reached in Biomet Vanguard Knee Replacement Lawsuit August 14, 2025 Zimmer Biomet Bone Cement Lawsuit Filed Over Failed Knee Replacement July 10, 2025 0 Comments 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 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 SmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body (Posted: 2 days ago)A Missouri woman alleges her AngioDynamics SmartPort catheter fractured and left a broken piece near her heart, requiring surgical removal after it was found during a CT scan.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUIT18 AngioDynamics Port Catheter Lawsuits Will Be Selected for Bellwether Discovery in August 2026 (05/05/2026)AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism (04/30/2026)Vortex Port Lawsuit Filed After Port Catheter Removed Due to Infection, Blood Clots (04/09/2026) Enfamil NEC Lawsuit Cleared For MDL Trial in July 2026 (Posted: 3 days ago)A federal judge has selected an Enfamil lawsuit to serve as the first NEC infant formula bellwether trial, which is set to begin in July.MORE ABOUT: ENFAMIL AND SIMILAC BABY FORMULA LAWSUITLawsuit Claims Cowโs Milk-Based Baby Formula Use Resulted in Infant Suffering Devastating NEC Symptoms (05/08/2026)Mead Johnson Lawsuit Claims Premature Child Developed NEC From Enfamil (04/24/2026)Similac NEC Lawsuit Payout Increased by $17M in Punitive Damages (04/14/2026) Abbott Eterna Lawsuit Alleges Spinal Cord Stimulator Malfunction Resulted in Worsening Pain (Posted: 4 days ago)According to a lawsuit brought against the manufacturer and the FDA, an Abbott Eterna spinal cord stimulator has caused pain, shocks and complications instead of the relief promised.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Stimulator Lawsuit Alleges SCS Lead Failure Caused Nerve Damage (05/06/2026)Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (04/29/2026)JPML Sets Hearing Over Spinal Cord Stimulator Lawsuit Consolidation for May 28 (04/24/2026)
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