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.
Chlorpyrifos Parkinsonโs Disease Lawsuit Chlorpyrifos lawsuits are being investigated for individuals diagnosed with Parkinsonโs disease after direct, residential, occupational or Gulf War pesticide exposure.
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
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.
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.
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.
Stryker Shoulder Pain Pump Lawsuit Settled Days Before Trial February 13, 2012 Staff Writers Add Your CommentsStryker Corporation has reached an agreement to settle a shoulder pain pump lawsuit brought by six people who allege that they suffered permanent damage to the cartilage in their shoulder after using one of the company’s devices to deliver pain medication after arthroscopic surgery.ย A lawsuit brought by Erika Creech, David Elder, Tyler Jones, Cody Thygesen, Julie Olsen and Jordan Schweizer was settled 18 days ago, resolving the case before a trial that was scheduled to begin today.The settlement agreement came less than a month after a federal judge in Utah rejected Stryker’s attempt to have the 2007 complaint thrown out. Terms of the settlement have not been disclosed.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 COMPENSATIONAccording to the complaint, all of the plaintiffs received a Stryker pain pump following shoulder surgeries between February 2003 and February 2004. Plaintiffs allege that the combination of drugs delivered directly into their shoulder joints during the days after surgery caused the cartilage to deteriorate.Known as chondrolysis, the painful and permanent loss of cartilage can cause decreased range of motion, pain, popping and grinding of the joint, which often leads to the need for a total joint replacement.ย The complaint is similar to a number of other shoulder pain pump lawsuits currently pending in courts throughout the United States against Stryker and other manufacturers of similar devices, including I-Flow, Breg, DePuy, Inc. and Smith & Nephew, Inc.In November 2009, the FDA required manufacturers of the pumps and the local anesthetics used with the devices to add new warnings about the risk of chondrolysis from should pain pumps. The warnings were designed to alert healthcare professionals that the use of pain pumps following shoulder surgery to infuse medication directly into the joint increases the risk of chondrolysis, particularly involving the shoulder. Tags: Chondrolysis, Glenohumeral Chondrolysis, Pain Pump, Shoulder, Shoulder Chondrolysis, Shoulder Pump, Stryker Image Credit: |More Lawsuit Stories Dupixent CTCL Studies Highlighted Cancer Risks For Years, Lawsuit Alleges August 11, 2026 Enfamil Necrotizing Enterocolitis Lawsuit Set for Trial to Begin This Week August 11, 2026 Gree Dehumidifier Lawsuit Alleges Defective Appliance Caused House Fire August 11, 2026 7 Comments Rick July 10, 2023 I had should pain pump that ate my cartilage and now need a shoulder replacement at 45, anything I can do? Hollis March 11, 2023 Paine at all times tenden tears and rceded movement restricted weakness some swelling Juan January 31, 2023 2003 had shoulder orthopedic surgery I was working for the city of Phoenix AZ water department injury they took good care of me through work man comp. Sent home with pain pump I remember doctor telling me this pain pump is a new thing we’re using. Didn’t make it through therapymy shoulder froze up could not move it few Months later he had to redo surgery sent me home again with another pain pump. I tried to complete my therapy but was not able to go back to work. Lost my home my job now I’m on disability please help Thank you. Katherine September 22, 2021 I had a hip replacement done and had a Stryker pain pump that caused the cartilage in my hip to deteriorate at 27 years old I had to have 2 full hip replacements Dan April 1, 2021 I have gotten shoulder orthopedic surgery in Roaring Springs PA and 2006. I am pretty sure I used i-flow pain pump it was in my arm for at least a week or longer. I was young at the time I did not know there was a settlement I did not know all these companies got sued as well. I don’t know who to contact or turn to for help my shoulder constantly pops and constantly in pain. I can provide all the right documents to prove my statement. Can someone please help me and let me know who I have to contact if I have a settlement or money. In a treasury for me. Years ago I got a piece of paper in the mail saying that I might have compensation due to the FDA not approving the pain pump I filled it out and I never heard anything back Jeff December 3, 2020 My name is Jeff and I had a shoulder replacement 02/24/2004 and also had the Stryker pain pump that was recalled. I’m 45 years old and have severe cartilage deteriation in my shoulder. I had an MRI and all kinds of test done and I have the arthritis of an 80 year old man. I don’t know what to do. IV been in pain for years and im sick of it. Please someone help me!! Carri February 11, 2020 I am caregiver for Brandi Kiser dob 3/26/84 she had Shoulder surgery 12-13 years ago using the after surgery pain pump at CMH in Boliver MO. We went to Mercy Orthopedic surgeon in Springfield MO Dr Seafall III today and he stated her shoulder looks like at 80 year old and she is only 35 he has never seen such deterioration on such a young person she was a 1%er they donโt ever see. Brandi has many mental health medical diseases which prevent her from handling this kind of thing on her own and she is also On disability. She was devastated to learn they can not repair her shoulder only replaced it. She has no transportation only a few people who helps her and now she is going to have to go to pain management clinic until we can get her into a major medical surgery facility about 3-5 hours away for shoulder replacement surgery and itโs likely she will require another since she is so young and the replacement are not designed to last her lifespan. She deserves to be compensated for her medical and pain/suffering she is experiencing and whatโs to come in near future and additional surgeries to come in her far future. 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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 Dupixent CTCL Studies Highlighted Cancer Risks For Years, Lawsuit Alleges (Posted: yesterday)A Dupixent CTCL lawsuit indicates manufacturers have long known the eczema treatment was linked to an increased cancer risk, but failed to warn doctors or patients.MORE ABOUT: DUPIXENT LAWSUITCTCL Lawsuit Alleges Diagnosis Came After Less Than a Year of Dupixent Use (07/29/2026)Lawsuit Alleges Dupixent Caused Mycosis Fungoides Diagnosis (07/21/2026)Dupixent MDL Judge To Meet With Lawyers for Initial Case Management Conference in October 2026 (06/25/2026) Abbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims (Posted: 2 days ago)Manufacturer wants the Judicial Panel on Multidistrict Litigation to reject a proposal by a group of plaintiffs to consolidate all federal Abbott spinal cord stimulator lawsuits.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (08/06/2026)Spine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026)Spinal Cord Stimulator Reprogramming Caused Electric Shocks, Worsening Pain: Lawsuit (07/27/2026) AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis (Posted: 5 days ago)A Pennsylvania man has filed an AngioDynamics SmartPort lawsuit alleging catheter defects promoted bacterial growth, causing a severe infection and sepsis only weeks after implantation.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Sepsis Lawsuit Claims Defective SmartPort Implant Caused Infection (07/22/2026)SmartPort Catheter Lawsuit Claims Defective AngioDynamics Port-a-Cath Caused Infection (07/14/2026)Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (07/07/2026)
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