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.
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
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.
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.
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.
Lawsuit Filed Over Fractured M-Cor Hip Replacement Implants May 25, 2012 Austin Kirk Add Your CommentsAn Arizona man has filed a product liability lawsuit after both of his hip replacements failed when M-COR hip implant components fractured inside his body.ย The complaint (PDF) was filed by William Fraze and his wife, Anna, in the U.S. District Court for the District of Arizona on May 21. Defendants named in the lawsuit include Portland Orthopedics Limited, Plus Orthopedics, Smith & Nephew, Inc., Maxx Health, Inc., Mipro US, Inc. and Encore Medical Corporation.According to allegations raised in the hip replacement lawsuit, Fraze received an M-COR femoral neck and femoral stem as part of his artificial hip systems implanted into his left hip in June 2007 and into his right hip in August 2007.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 COMPENSATIONIn April 2010, Fraze alleges that his left hip implant broke, causing a large knot to appear and resulting in excruciating pain with even slight weight. An x-ray revealed that the M-Cor femoral neck component of the left hip had fractured, which was confirmed during revision surgery that same month.Only a few months after that surgery, in August 2010, Fraze heard a snap in his right hip, which caused his leg to give out and prevented him from bearing any weight on his right leg. X-rays revealed that the femoral neck of the M-COR implant had dislocated, and following revision surgery on his right hip it was discovered that the proximal neck of the hip stem had fractured on that side as well.The M-COR hip implant was developed in 1991 by Professor Ron Sekel and Portland Orthopedics Limited in Australia, according to the lawsuit. Portland Orthopedics began selling the M-COR after receiving FDA pre-market approval in 2006. Plus Orthopedics, which was eventually absorbed by Smith & Nephew, was the U.S. distributor for M-COR hip implants. Encore sold numerous components that were implanted with the M-COR. In 2009, Plus Orthopedics was acquired by Maxx Health, Inc.According to allegations raised in the complaint, the M-COR components implanted in his hips were defective. The predecessor for the components, the MARGRON DTC Hip Replacement System, was recalled in Australia in 2008, due to a higher-than-normal revision rate. At the time, Portland Orthopedics recommended regular monitoring for all patients who received their M-COR implants in the United States.Fraze seeks damages for physical and mental pain and suffering, physical impairment, physical disfigurement, past and future medical bills, loss of earning and earning capacity. His wife is suing for loss of consortium and loss of household services. Tags: Arizona, Hip Replacement, Product Liability, Smith & Nephew Image Credit: |More Lawsuit Stories DraftKings Gambling Lawsuit Alleges Illegal Scheme Fueled Addiction October 27, 2026 Snapchat Child Sexual Abuse Lawsuit Alleges Predator Targeted 9-Year-Old Girl October 27, 2026 Olympus Scope Problems Lead to FDA Import Warning October 27, 2026 4 Comments Karlen July 5, 2017 I am currently in the hospital awaiting a revision surgery for a failure of the same implant. Can you give me any helpful information about proceeding with legal action? Did your doctor monitor your implant following surgery? Karlen John May 6, 2016 Is there a class action in the pipeline for Australia hip failures? Julia December 19, 2014 hip replacement Kazi June 27, 2012 Hello I have similar medical problems with the Margaron Hip replacement and Portland Orthopedics Limited. I’d like to know how to keep a track on the outcome of this case and if there is anything that can be done for Australian citizens that are also experiencing extreme difficulties with the same product and company. I’m now on my fifth hip replacement because of the faults with this prosthesis and many others in Australia are also suffering. If you are unable to help Australian citizens, could you at the least tell me how I can find out about the outcome of this case, which may help me with my own action. Thank you for your help and for posting this issue. Regards Kazi PhoneThis 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. 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