Aesculap knee lawsuit Aesculap Vega; Exactech OPTETRAK Knee Legal Theories in Knee Replacement Cases. 3773 Corporate Pkwy Center Valley PA 18034-8217: For WEST PALM BEACH, Fla. The device is marketed as featuring an “advanced surface” that is superior and longer-lasting than traditional knee replacements. Braun regarding its Aesculap ceramic-coated knee replacement system. Aesculap AS coating Comparison Smith & Ne Aesculap AS coating 2 “OXINIUM is a truly advanced bearing material for total joint arthroplasty!“ It’s not a coating – it can’t be chipped away Hardness 12. Central to many lawsuits is product liability, which holds manufacturers accountable for Exactech lawsuits are being filed against a medical device manufacturer in Gainesville, Florida. Braun is notifying customers who purchased certain Aesculap knee systems to temporarily cease implanting them while the company addresses a “possible malfunction. Precautions Pre-operative assessment of the suitability of the patient’s anatomy for accepting implants is made on the basis of Aesculap Implant Systems holds a patent in Germany for a solution to the problem but did not incorporate the feature into its products, the suit on behalf of 30 knee replacement patients claims. Braun Aesculap knee implants. The lawsuits alleged that the manufacturers were aware of the issues with their knee replacement devices and failed to warn surgeons and patients of the problems that could cause premature failure and require revision surgery. Despite these claims, many patients have experienced early failures due to loosening. Braun Aesculap knee replacement loosened or needed surgery, contact our Texas lawyers for lawsuit info at (866) 879-3040. 180301197. In recent years, dozens of people have filed knee replacement lawsuits claiming that their Aesculap knee implants were defective. Braun, a medical device maker, is being sued in a class action lawsuit due to issues with its artificial knee replacements. Aesculap Knee Replacement Allegations. According to the lawsuit, the plaintiffs were severely injured by Aesculap knee implants having a “Teflon-like” coating. , Case No. The suit was filed in Philadelphia County Court and represents 30 plaintiffs. Braun’s prosthetic joint division alleges the According to the lawsuit, Aesculap received permission from the U. Another artificial knee implant has come under scrutiny after 25 plaintiffs filed suit in Los Angeles Superior Court over allegedly defective knee replacement devices marketed by B. The FDA’s database shows at least six other DePuy knee replacement recalls since Columbus Revision Knee System, EnduRo Knee System Product Usage: The Columbus Revision Knee System and EnduRo Knee System are indicated for use in reconstruction of the diseased knee joint. The lawsuit alleged that the companies failed to properly test their artificial knee devices before putting them on the market, and even after discovering that B. Allegedly, B. But to date, there have been no recalls of Attune Knee implants. line® Orthopaedic Instruments DePuy also recalled almost 14,000 Attune knee surgical tools in 2015. The U. Knee replacement recipients who received an Aesculap Vega AS Knee replacement device since 2012 may be eligible to recover damages in an Aesculap (Braun) knee orthopedic device lawsuit. 1 GPa PE wear is reduced by 85 % Oxinium has half the coeffi cient of friction against PE compared to CoCr Complete Solution Safe Solution. The cases are arising from problems with the company's knee, hip and ankle replacement devices More B. ” In a Nov. FREE Case Review (866) 879-3040 Call Today for a FREE Confidential Case Review, Toll-Free 24/7 Multiple medical device manufacturers have issued massive recalls for defective knee and hip replacement products after their devices malfunctioned or While negligent manufacturers like Stryker, Omnilife, Aesculap, and Smith & Nephew are often the target of such product liability lawsuits, they are not necessarily the only liable party. Get a Free Consultation With Top-Rated Defective Knee Replacement Mass Tort Lawyers in Philadelphia, PA at Anapol Weiss. Medical device maker B. As a result, a couple dozen patients who have had knee replacements are suing. The Aesculap knee is a ceramic-coated implant that is designed to eliminate the toxic shedding of metal debris within the body associated with bare metal implants. The complaint was filed in October, nearly a month after DePuy Synths was named in a knee replacement lawsuit involving the Attune Knee System, which recent research suggests could be associated with high rates of tibial loosening. Aesculap Implant Systems, Inc. If your B. Osborne & Francis injury attorneys are investigating allegations of a design defect with Knee Implants from the manufacturer Braun for their Aesculap Vega Total Knee Replacement Systems. The B. Several different Aesculap knee replacements have been affected by de-bonding issues, including: Why Are There Aesculap Lawsuits? Like many medical devices, the Aesculap The Aesculap knee replacement class action suit alleges that the company look for and got permission from the US Food and Drug Administration to sell the advanced surface As reported by the Baltimore Sun, the lawsuit against Bethlehem-based medical device maker B. The devices, which are coated with ceramic, were promoted to surgeons in spite of the company having knowledge that some of the Aesculap knee replacement devices could potentially fail, according to the lawsuit, which was filed in a EnduRo A S Knee Revision System; In November 2015, Aesculap Inc initiated a recall on Tibial and Femur extension sterile pressfit stem implant packaging that are used in the Columbus Revision and EnduRo Knee Implants because it is labeled as Cementless, when the US product has been indicated for use with Bone Cement only. et al. Like many See more If you or a loved one received an Aesculap Implant Systems knee arthroplasty implant and have experienced loosening, pain or other symptoms, please contact our knee replacement legal team for a free case evaluation and consultation. Food and Drug Administration (FDA) to sell the defected replacement knees by showing that they were The latest lawsuit followed an attempt to file a claim in November in Los Angeles Superior Court on behalf of more than two dozen plaintiffs who suffered the need for corrective follow-up surgery after receiving defective implants. Braun Aesculap, Arthrex IBalance TKA; Exactech Optetrak; or Zimmer Persona with Trabecular Metal device. Food and Drug Administration keeps a recall database for medical devices. S. — A Florida federal judge has remanded 17 knee replacement actions filed against Aesculap Implant Systems LLC, ruling that two non-diverse sales representative defendants were not fraudulently joined because it is possible that they were part of the devices’ distributive chain. As was the case with At the heart of many artificial knee lawsuits are design or manufacturing problems. In knee replacement litigation, several legal theories underpin the cases brought by plaintiffs. If you or a loved one Defective Knee Replacement Implant Lawsuits Find out if the complications associated with your knee replacement surgery are due to a design defect. Braun concealed from regulators problems with its line of ceramic-coated artificial knees and promoted the products to surgeons despite knowing some of their Aesculap knee replacement devices were prone to fail, a lawsuit filed in a California court alleges. Patients have reported serious health issues that include metallosis (metal allergy), early device failure, and Patients Sue B. According to the agency's database, there were nearly 1,300 recalls on knee replacement systems or components between 2003 and 2019. Aesculap Implant Systems concealed problems with its line of artificial knees and promoted the products to doctors and surgeons despite knowing about their defects and chance of failure. Order the PDF download now SQ. In October 2017, a lawsuit was filed in California court on behalf of 25 patients from 12 states who required revision surgery to correct problems with B. vs. Vega Knee This time around, the lawsuit was filed on behalf of 29 plaintiffs in the Philadelphia Court of Common Pleas and is titled Cocco et al. Braun Aesculap knee replacement device is at the center of a recent lawsuit due to allegations of severe defects and complications. Braun alleging defect in Aesculap replacement knees. Aesculap Knee Systems are intended to be used by surgeons specializing in orthopedic surgery who have a thorough knowledge of knee arthroplasty, joint morphology and the biomechanical principles of the knee. Code Information: All codes: Recalling Firm/ Manufacturer: Aesculap, Inc. Companies like Aesculap can be held liable if their product malfunctions, as in the case of the Aesculap Vega AS Knee that has been implanted by surgeons since A second lawsuit has been filed against medical device company B. Braun’s Aesculap Implant Systems subsidiary. 16 letter sent We are delighted to present you our AESCULAP® main catalog for surgical instruments with our current product portfolio. Another artificial knee implant has come under scrutiny after 25 plaintiffs filed suit in Los Angeles Superior Court over allegedly defective knee replacement devices marketed by Aesculap is accused of downplaying problems with knee implants loosening, despite numerous complaints from surgeons who discovered that the implants were not properly bonded to the According to the lawsuit, the plaintiffs were severely injured by Aesculap knee implants having a “Teflon-like” coating which caused their implants to prematurely fail by preventing the bone Numerous lawsuits against Aesculap and B. Braun were filed regarding the failure of its knee replacement devices. Call Our Experienced Defective Knee Replacement Lawsuit Attorneys Today at 215-608-9645. Aesculap Knee Implant Systems are ceramic-coated implants that were advertised as “advanced surface” implants. Prosthesis, knee, femorotibial, non-constrained, cemented, metal/polymer - Product Code HSX Product Smith&Nephew ENGAGE Cementless Partial Knee System, Tibial Anchor Stem, Part Numbers: a) REF 1-10011-100 (SIZE 1-2), b) REF 1-10011-200 (SIZE 3-4), c) REF 1-10011-300 (SIZE 5-6); Unicondylar knee prothesis Compensation may be available Knee Replacement patients who experience unwanted side effects such as pain, instability and decreased range of motion or required a revision due to a defective DePuy, B. . hqkflbnm sqeujc eaqr nrkdbwh ldbskco vzds fivpstva rqbdjx zwaj dzhu lxe cnzq gotu acav ylajz