Some artificial knee implants have been associated with pain, instability, limited range of motion, and premature failures that led to unplanned, additional operations. When a large corporation appears to be profiting at the expense of American consumers, our DePuy attorneys see it as their mission to pursue justice and push the company toward greater corporate responsibility. After various treatments,MD recommended TKR. When they fail this duty, those who are injured by those products have a right to hold the manufacturers accountable for their injuries and resulting damages. Because of the high rate of failures that have been associated with the Attune Knee System, patients with these artificial knees should know the symptoms of device loosening, breakage, and failure: Any patient who has an Attune implant should make an appointment to have their knee assessed if they experience any of the above symptoms. At least 500 reports of malfunctions, adverse events, failures, and revision surgeries have been reported to the MAUDE database in the first eight months of 2018 alone. NOTE: Providing information for review by an attorney does not form an attorney-client relationship. Another study published in 2017 in the Journal of Knee Surgery warned that the FDA had received an unusual number of complaints linked to tibial loosening and failures. More lawsuits are expected to be filed against DePuy and Johnson & Johnson related to the Attune Knee Replacement System. Read full, Our DePuy knee attorneys have extensive experience and a strong track record winning product liability cases for defective medical devices including DePuy joint replacement systems. These injuries occurred during normal walking activities. Site Sponsored by: Saiontz & Kirk, P.A. The “AOX Polyethylene” is a plastic material that is designed to replace cartilage in the knee, which can help improve the device’s strength and resistance to wear. During only a two-month period, the FDA received at least 21 adverse event reports involving DePuy Attune knee failures, which likely only represents a small fraction of the actual number of problems experienced by individuals who received this implant system. Researchers examined FDA reports in the Manufacturer and User Facility Device Experience (MAUDE) database related to Attune devices. If the knee has broken, loosened or otherwise failed, contact us to learn more about your rights including the right to seek compensation. Any patient who suffers device loosening, malfunctions, or a premature failure that leads to unplanned, revision surgeries has the power to hold the manufacturer accountable, and we help make sure the playing field is equal, no how big that manufacturer may be. The Class II Device Recall dealt with more than 3,000 units. This early rehabilitation will also help flexibility and range of motion. Below is a partial list of the awards and recognition that the attorneys / lawyers at our law firm have been awarded with, as well as a list of professional memberships. We are very proud of our legal achievements, but equally self-respecting of our firm's reputation for providing personal attention to each and every client we represent. According to the FDA, “a claim of substantial equivalence does not mean the new and predicate devices must be identical.” A device must only be equivalent in design, use, and others. The firm cited the study in the Journal of Knee Surgery as evidence of the high failure rates. Thus far, there have been multiple DePuy knee recalls for particular DePuy knee components, including the meniscal bearing insert in the LCS knee system and the LPS Lower Extremity Dovetail component. Although there are benefits to joining a class action lawsuit, you may actually be able to maximize your recovery by seeking individual legal representation and filing a personal injury lawsuit. The U.S. Food and Drug Administration (FDA) announced the recall in the following Safety Communication. DePuy knee replacement systems should last approximately 15 years. Patients often present with pain on weight bearing, swelling, and decreased range of motion. Women have reported problems where Paragard IUD fractured or broken during removal, resulting in serious injury. They allege that the Attune knee implant is more dangerous than other implants, is not effective, raises the risk of serious injury and that DePuy failed to warn the medical community and patients about these defects and risks including that the implant may fail within two years of being implanted. Calls Answered 24 Hours Read full. Talcum powder or talc powder may cause women to develop ovarian cancer. That’s what happened in thousands of patients who underwent a total knee replacement with DePuy Synthes Attune Knee Replacement System. DePuy knee replacement lawsuits against the subsidiary of Johnson & Johnson are the best means for individual consumers to hold the pharmaceutical giant accountable. But, when these devices don’t work as they should, life can be very difficult for the recipient. And some of the devices that Attune showed its similarity too include: But these devices had problems of their own, including two recalled for malfunctions and failures. Even if the surgery is successful, the patient can experience complications as soon as two years after the device was implanted. Unfortunately, unexpected complications are not out of the ordinary. We are currently investigating cases involving individuals who have undergone revision surgery due to loosening after a knee replacement using an ATTUNE device. When the FDA checks to see if a new device is substantially similar to a predicate device, it doesn’t conduct a look-back at its history, so it doesn’t matter if the predicate device has been recalled or if it has been linked to serious complications and adverse events. After examining the explanted devices, the study authors found that the cement bond between the leg bone and the baseplate of the device had broken. Attorneys handling national DePuy knee lawsuits believe that persons who have been harmed by a faulty DePuy knee replacement or forced to undergo knee revision surgery may be entitled to significant compensation through filing a claim against the Johnson & Johnson subsidiary. The lawsuit was filed in September 2017 in the Circuit Court of Tuscaloosa County by Cunningham Bounds LLC. Negative Pressure Wound Therapy (Wound Vacuum), PPI (Proton Pump Inhibitor) Stomach Cancer, Malfunctions and Premature Failures with Attune Knee, reports of malfunctions, adverse events, failures, and revision surgeries, Instability or a knee that shifts backward, forward, or sideways upon standing, Inflammation and swelling of the knee joint after you have fully recovered, Infection deep within the joint or surrounding the implant, Heat and redness surrounding the knee joint. The Schmidt Firm, PLLC is nationally recognized as a class action law firm. Contact us today to learn more about holding DePuy accountable for Attune Knee System injuries, failures, and revision surgeries, and whether you are entitled to significant financial compensation for your injuries. If you have claim, we will start immediately. Should you choose to retain our DePuy knee attorneys, there is never any fee unless we win compensation on your behalf. Since its release almost a decade ago, it has been used in more than 400,000 knee replacement procedures. So far, there has not been a recall of the Attune system, despite reports of high rates of failure. Persons who were implanted with a faulty DePuy joint were awarded, on average, over $300,000 each for the pain, medical bills, and rehabilitation time they suffered. An MDL transfers individual lawsuits from many state courts to one federal court, centralized under one judge. DePuy knee failure symptoms include pain, heat at the joint, hyperextension, knee instability, and swelling. According to the American Academy of Orthopaedic Surgeons, these are the most common causes of knee pain that require knee replacements: During knee replacement surgery, cartilage is removed before metal components are added to the surface of the joint. The Agency for Healthcare Research and Quality reports that more than 600,000 knee replacements are performed every year in the United States alone. (866) 280-4722, © 2018 Drug Lawsuit Source, All Rights Reserved | Call (866) 280-3417 For Free Case Review | Privacy Policy | Sitemap. The Attune Knee System, manufactured by Johnson & Johnson subsidiary DePuy, is advertised and promoted as having certain technologies that make it more stable than other devices. Faulty DePuy knees require revision surgery, which is more complex, painful, and invasive than typical knee replacement surgery. In December 2010, the DePuy Attune Knee System was approved by the U.S. Food and Drug Administration under the agency’s 510(k) approval process. After that, you will need to avoid certain activities such as high-impact sports and running for the rest of your life, but low-impact sports and activities like walking, swimming, and biking are encouraged. Attorneys handling DePuy knee failure lawsuits work on contingency, meaning you never pay legal fees unless we win compensation for you. When the pain becomes too severe, sometimes a total knee replacement is the only option.

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