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.
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.
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.
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.
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.
Change Healthcare Lawsuit Lawyers are reviewing Change Healthcare class action lawsuits for individuals who had their personal information stolen due to the data breach.
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.
AngioDynamics Port Catheter 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.
Processed Food Lawsuit Lawsuits are being pursued against the food industry over their manufacturing and advertising of ultra-processed foods, which have caused a generation of children to face an increased risk of developing childhood diabetes and other chronic illnesses.
MRI May Detect Metal-on-Metal Hip Tissue Damage: Study May 21, 2013 Irvin Jackson Add Your Comments Magnetic resonance imaging (MRI) exams may be used to detect developing problems with metal-on-metal hip replacements before patients start showing symptoms, according to a new study.  Researchers from the Hospital for Special Surgery published a study in the Journal of Bone & Joint Surgery, which indicates that joint inflammation was present in most patients with failed metal-on-metal hip replacement systems long before other symptoms appeared. That inflammation of the joint lining, known as synovotis, can be detected by an MRI scan. The investigators looked at 69 patients with a total of 74 artificial hips. They looked at patients who had hip problems but were asymptomatic, symptomatic with a known mechanical cause and those patients with unexplained pain. Synovitis was found in the majority of all the patients, but it was only statistically significant in patients suffering adverse local tissue reactions. Learn More About Hip Replacement Lawsuits Lawsuits are being reviewed for several different dangerous and defective hip replacement systems. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Learn More About Hip Replacement Lawsuits Lawsuits are being reviewed for several different dangerous and defective hip replacement systems. Learn More SEE IF YOU QUALIFY FOR COMPENSATION “Synovial volume on MRI may be a valuable marker in the longitudinal assessment of asymptomatic patients with a metal-on-metal hip resurfacing and in identifying patients with adverse local tissue reaction,” the researchers concluded. Concerns About Metal-on-Metal Hip Problems Concerns have surfaced in recent years that metallic debris from metal-on-metal hip implants could cause tissue damage and metal blood poisoning, also known as metallosis. In many cases, these problems have caused individuals to experience problems where their hip replacement loosens or fails catastrophically and ultimately needs to be replaced. In January, the FDA released new guidance for metal-on-metal hip replacements. The agency told doctors that metal-on-metal hip replacement systems should only be used if other artificial hip implants were not appropriate, and called on manufacturers to prove that their implants were safe enough to stay on the market. Future metal-on-metal hip designs will have to undergo extensive human clinical trials before being made available for sale, the FDA decreed. The agency also provided updated information for orthopedic surgeons, advising that doctors should pay close attention to patients with metal-on-metal hip replacements and to look for signs and symptoms of common problems associated with those artificial hips. Metal-on-Metal Hip Lawsuits A number of metal-on-metal hips have been recalled, targeted by patients who say they were sold defective artificial hips, or both. In August 2010, Johnson & Johnson issued a recall for the DePuy ASR metal-on-metal hip system, after data suggested that as many as one out of every 8 implants were failing within five years. However, by the time the hip replacement was removed from the market more than 90,000 of the components were sold worldwide. Johnson & Johnson now faces thousands of DePuy ASR lawsuits. So far this year, two cases have gone to trial, with one case in California resulting in an $8.3 million damage award and a second case in Illinois state courtresulting in a defense verdict. In addition, a growing number of lawsuits have been filed over other metal-on-metal hip systems, including the DePuy Pinnacle hip, Biomet M2A Magnum hip and Wright Medical Conserve Cup. Tags: Biomet M2A Magnum, Depuy ASR Hip, DePuy Pinnacle Hip, Metal Hip Replacement, Metal-on-Metal Hip Replacement, MRI, Wright Conserve Hip Implant Image Credit: | More Hip Replacements Lawsuit Stories Biomet Hip Lawsuit Filed Over Defective M2A Metal-on-Metal Implant December 26, 2024 Zimmer Biomet Lawsuit Filed Over RibFix Blu Implant Fracture September 25, 2024 Zimmer Biomet CPT Hip System Linked to Increased Risk of Thigh Bone Fractures, FDA Warns September 18, 2024 1 Comments Howard May 21, 2013 Smith & Nephew’s Birmingham hip resurfacing device isn’t mentioned yet figures indicate this device has failed in a much higher than acceptable rate. The only data and reports are from Smith & Nephew. They have touted how successful their device is when compared to other resurfacing devices. What they neglect to tell folks is the other two PMA approved resurfacing devices are hardly used, thus making the results they tout unrealistic. Are we to allow Smith & Nephew and the BHR to go unnoticed ? I hope not, this manufacturer is no innocent lamb they are repeat offenders of kickback laws in the USA and abroad, they are presently in court being sued by the United States of America on a whistleblower case. The approval of their Birmingham hip resurfacing device was a farce, it was an indication of the ongoing corruption in the medical device world and an example of the inadequacy and ineptness of the FDA and their approval process. They approved this device with unknown information as to the metal particles, caused from friction of the components, and the results it may have on a human being. They ignored the fact the investigator, inventor, employee of Smith & Nephew received 66 million pounds for his company. The only asset the company, Midland Medical Tech had was the Birmingham hip. Then the same person received an additional 33 million pounds upon the PMA approval by the FDA. Respectfully Howard 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 No Post Comment I authorize the above comments be posted on this page Weekly 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 TermEmailThis field is for validation purposes and should be left unchanged. Δ MORE TOP STORIES Wrongful Death Lawsuit Links Oxbryta Side Effects With Deadly Vaso-Occlusive Crises (Posted: today) A wrongful death lawsuit claims a Tennessee man suffered severe Oxbryta side effects, leading to stroke, complications and death. MORE ABOUT: OXBRYTA LAWSUITOxbryta Recall Lawsuit Alleges Sickle Cell Drug Increased Frequency of Dangerous VOCs (05/23/2025)First Oxbryta Lawsuit Set for Trial in August 2027, Over Recalled Sickle Cell Drug Risks (05/09/2025)Malpractice Lawsuit Alleges Side Effects of Oxbryta Caused Untimely Death (04/15/2025) Lawsuit Claims Biozorb Implant Penetrated Skin, Causing Massive Infection (Posted: yesterday) A BioZorb lawsuit claims that the recalled implant’s defective design led to the device migrating through a woman’s flesh, causing a severe infection. 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Zimmer Biomet CPT Hip System Linked to Increased Risk of Thigh Bone Fractures, FDA Warns September 18, 2024
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More Than 1,700 Bard PowerPort Lawsuits Now Filed in State and Federal Courts (Posted: 2 days ago) As the number of Bard PowerPort lawsuits brought over design defects associated with the port catheter system continues to mount, lawyers have agreed on the first bellwether case that should go before a jury. MORE ABOUT: BARD POWERPORT LAWSUIT6 Bard PowerPort Lawsuits Selected for Bellwether Trials in Federal MDL (05/19/2025)Court Indicates Bard PowerPort MDL Bellwether Lawsuits Should Include 3 Infection, 2 Thrombosis and 1 Fracture Case (05/06/2025)Lawyers Proposed 11 Bard Implantable Port Catheter Lawsuits as Bellwether Trial Candidates (04/30/2025)