Zimmer Nexgen Knee Replacement Recall

There has been a constant demand for Zimmer NexGen knee replacement recall from doctors and patients in a similar fashion. Overview of the most common implants for total hip and total knee arthroplasty. The Persona knee implant is the newest in Zimmer's line of knee replacement products. 4 This one judge would then organize and administer the discovery process for all Zimmer NexGen Knee Replacement cases until the case is ready for trial. Senator Chuck Grassley has also inquired into the reliability of the products Zimmer continues to put on the market. While Zimmer markets a number of knee implants, its NexGen devices have come under fire due to allegations of a high failure rate and a series of FDA product recalls. The Zimmer knee recalls in 2010 informed the public of potential problems linked to the NexGen product line, and in turn warned affected patients that their knee complications may not be normal. Recently, doctors have urged the FDA to recall the Zimmer NexGen knee replacements for failure rates higher than expected. In 2010, the company recalled 70,000 MIS Tibial components due to loosening issues. 1:11-cv-05468 ) ) Honorable Rebecca Pallmeyer ZIMMER’S RESPONSE TO PLAINTIFFS’ BELLWETHER SELECTIONS For three years, Plaintiffs have complained that Zimmer, Inc. That system uses a component that attaches to the bottom of the thigh bone without applying traditional cement to glue it in place. The next time I saw my surgeon, I said how can the Mayo Clinic give me a prostectic knee that is on recall. Knee replacement (also known as joint arthroplasty) surgery is a pretty common medical procedure which has increased quite a bit in the last few years. The defective Zimmer NexGen CR-Flex product that have caught class action networks lawyers attention is a Femoral Implant. The product is used as an implant for knee replacement. The researchers found that nearly 9% required revision surgery and that 36% showed signs of the replacement knee loosening, concluding that the Zimmer NexGen knee problems were linked to the design. In 2008, Zimmer issued a voluntary recall of its metal-on-metal hip device, the Durom® Cup, and in 2010 issued another recall for the NexGen® MIS™ Tibial Components. Zimmer Holdings, Inc. Zimmer Knee Replacement Recalls. over the NexGen Complete Knee Solution MIS Tibial Components, Locking Screw and Stem Extensions, affecting 68,383 devices that had already been implanted. Introduced in 2003, Zimmer’s NexGen CR-Flex Porous Femoral Component is a synthetic device used to cap the thigh bone (femur) where it connects with the tibia at the knee. 2 by each plaintiff or their personal representative. Despite Zimmer's claims that its NexGen Knee Replacement products, such as the NexGen CR, are the best performing of all major knee replacement systems, said has unfortunately received quite a bit of public scrutiny, due to serious complications associated with its use, such as: Loosening or fracture of the implant components. Zimmer, Inc. Contact Bruno & Bruno While this website provides general information, it does not constitute legal advice. Zimmer Persona Issues Recall, Has History of Recalls for Various Products and Devices March 31, 2015 Zimmer, the largest manufacturer of knee implants, has recently recalled its Persona Knee implants after a substantial number of patients complained of pain and complications after the implants were used in their knee replacement surgeries. Zimmer Nexgen Protocol - Free download as PDF File (. Zimmer Recalls Persona Knee Replacements. Knee replacements are one of the most common surgeries done in the United States. Knee Replacement Patients Report DePuy Attune® Implant Loosening And Failure Knee replacement surgery, also known as arthroplasty, is a common orthopedic procedure used to relieve pain in patients whose knees have been damaged by debilitating arthritis, severe injury, or excessive wear and tear. delivers customizable implant combinations due to independent fit of each component and comprehensive instrumentation to aid surgeons in addressing diverse, often challenging procedures while choosing a personalized patient approach to revision knee surgery. Zimmer NexGen Knee Recall Zimmer Holdings, Inc. It was believed that this device was the best option for women due to superior fitting parts resulting in increased stability. Zimmer Inc. This high rate of implant failure is said to be due to design problems with the Zimmer NextGen CR-Flex replacement knees. Instead, an artificial knee is fused directly to the patient’s bone structure. For Zimmer Biomet sales representatives, you can log in to access more information Intra-operative systems that allow surgeon to accurately position the instruments and the implants iASSIST® Knee. The Zimmer NexGen MIS tibial component recall affected 68,384 knee components, which were distributed in 13 states across the U. All across the United States, the Zimmer NexGen knee replacement system is and continues to be a popular option among individuals in need of knee replacement surgery. Our track record of success speaks for itself. In all, 114 patients had to undergo knee replacement revision surgery due to these defective Zimmer components. If you’ve experienced complications arising out of your knee replacement, our experienced knee replacement lawyers are standing by to discuss your legal options with a free telephone consultation. Your Email. The truth is the Zimmer NexGen Knee Replacement System is clinically proven and the most trusted knee replacement system in the world. With the NexGen System, you have the power to create custom-fit solutions for primary or revision total knee arthroplasty. Knee replacements are intended to last approximately 15 years, but the Zimmer NexGen CR-Flex can reportedly fail within three years. It was in 1968 that Zimmer entered the knee implant market. Zimmer NexGen Knee Replacement Problems Reported March 31, 2010 Written by: Staff Writers 35 Comments; Orthopedic surgeons have released a new report that highlights the risk of problems with. The porous femoral component (that is, the part of the replacement that covers the head of the femur, the bone that goes from the pelvis to the knee) is associated with a high rate of failure. Food and Drug Administration can order a recall. According to the FDA, over 11,000 devices were. Zimmer Knee Replacement Recall Zimmer’s NexGen Complete Knee Solutions for knee replacement was recalled many years ago. The Zimmer NexGen knee replacement story is a sad one. The Zimmer knee recalls in 2010 informed the public of potential problems linked to the NexGen product line, and in turn warned affected patients that their knee complications may not be normal. Zimmer Knee Replacement Law Firm. Zimmer® NexGen® LPS Fixed Bearing Knee. The NexGen CR-Flex and LPS-Flex Fixed Bearing Knee, designed and manufactured by Zimmer Holdings, Inc. Zimmer knee replacement lawsuits are serious matters and you need a top product liability attorney on your side!. Berger's warnings, United States Senator Charles E. The Food and Drug Administration (FDA) issued a recall of the Zimmer knee in September 2010. According to the FDA, this recall affects 11,658 of these knee components worldwide. Total knee replacements should last between 15 and 20 years. Patients have reported intense pain and premature failure issues with the knee device. Wear-resistant polyethylene to help minimize osteolysis. over the NexGen Complete Knee Solution MIS Tibial Components, Locking Screw and Stem Extensions, affecting 68,383 devices that had already been implanted. Merchant Law Group LLP has launched class action litigation regarding knee replacement failure allegedly caused by defects in Zimmer NexGen CR and Zimmer NexGen CR-Flex Porous Femoral implants. Zimmer has released two knee implant models that are currently undergoing investigation due to the large number of problems reported by recipients. At least 114 adverse event reports involving loosening and revision surgery were reported at the time of the recall. Zimmer NexGen Knee was approved by the FDA in 1994, and since that time more than three million NexGen knees have been implanted worldwide. As a result of a Freedom of Information Act request submitted to the FDA, W&L was able to discover that the FDA had concerns about certain Zimmer Persona knee components which the FDA repetitively communicated to Zimmer prior to the initiation of these above-mentioned recalls. The attorneys at Bohrer Brady LLC are currently representing clients in knee implant litigation and can help you explore your legal options. has recalled thousands of components from the company's NexGen Complete Knee Solution and NexGen CR-Flex Knee Replacement products. Hi Dolores - I have the Zimmer next gen. The announcement from the FDA said that Zimmer was initiating a voluntary recall of the Persona knee implant. Our Galveston medical device lawyers recall news about a 2010 orthopedic surgeons’ conference that called attention to Zimmer NexGen knee replacements and Zimmer NexGen knee replacement components because of their “higher than expected” failure rates. Proner & Proner is a national law firm representing people injured by defective medical devices such as hip and knee replacements, including Zimmer knee replacement devices. Zimmer has had some safety issues with Persona and NexGen components, and other knee replacement devices, in the past. A significant number of patients who have received Zimmer NexGen CR-Flex knee implants have reported problems with the product. Welcome to the Persona Knee – putting the person back in knee replacement. Knee Replacement Complications. Zimmer distributed the recalled Persona Trabecular Metal Tibial plates in at least 25 states and at 13 major Veterans' Administration medical centers throughout the U. This product is known as the Zimmer Durom Cup. The complaints centered around loosened components, misalignment and very limited manufacturing defects. Zimmer Biomet has voluntarily recalled multiple devices over the years (Biomet recalled 25; Zimmer recalled 104). However, that same Australian data shows that the Zimmer NexGen LPS has the second highest revision rate of the 20 knee replacement devices listed -- nearly 60% higher than the average. The Zimmer NexGen Knee Implant was advertised as a product designed to accommodate resumption of high levels of activity. Zimmer NexGen recalls have been issued for several different parts that may be used in the company's complete knee replacement systems, including some Zimmer NexGen MIS and Zimmer NexGen LPS components. Kansas City Zimmer Knee Replacement Information Best Time to Seek Legal Help. Over the last decade, knee replacement surgery has become a popular and safe option for patients who have end-stage arthritis of the knee. The company has a negative history, first having done a voluntary recall of these knee replacement parts, as well as a metal-on-metal hip device (Durom Cup) and the Nex Gen MIS Tibial Components in recent years. Email Link. The reason for the FDA's recall of Zimmer NexGen complete knee solution MIS total knee procedure stemmed tibial component is eerily similar to problems now facing Zimmer with its NexGen CR-Flex. The Persona knee replacement system is a follow-up to the company's NexGen knee replacement system. I you believe you have taken all the proper steps to care for your implant and the failure is due to a faulty prosthesis, you should contact a Seattle knee recall attorney. Attune Knee Implant Raised Concerns. Zimmer Manufacturing initiated another sweeping recall on one of its artificial knee implants, because one of the pieces could loosen or fail because of shoddy manufacturing. Zimmer Knee Lawsuits. ’s NexGen Flex femoral. Knee Replacement Lawsuit: The Recent History of Faulty Knees. Potential Problems With Knee and Hip Implants. I have a Zimmer hip and when doing research for the implant and my OS, I had read about the Zimmer knee. Potts Law is accepting cases involving the Zimmer NexGen Flex knee system and Zimmer MIS Tibial Plate recall. Zimmer FDA Inspections Prior to Recall. This includes the 1995 release of the NexGen Complete Knee Solution System. In the 1990s, Zimmer introduced a line of total knee replacement devices, called NexGen, which helped pave the way for newer versions of its prosthetics that did not require clinical data for FDA approval. 4 This one judge would then organize and administer the discovery process for all Zimmer NexGen Knee Replacement cases until the case is ready for trial. The Persona knee replacement system is a follow-up to the company's NexGen knee replacement system. It is expected that this NexGen Knee Solution MIS Tibial Component recall may only be the beginning of wider potential recalls and failed knee surgery lawsuits as there are similar Zimmer NexGen knee products including Zimmer NexGen MIS, cementless Zimmer NexGen products, Zimmer NexGen Hi-Flex and Zimmer NexGen Gender Solutions that may have be. 3%, while 36% of patients fitted with the Zimmer knee replacement experienced significant loosening of the device. Zimmer Knee Replacement Class Action. Zimmer NexGen Knee was approved by the FDA in 1994, and since that time more than three million NexGen knees have been implanted worldwide. We offer market-leading knee replacement implants for partial knee and total knee arthroplasty for primary and revision procedures featuring our cemented and cementless flagship TKA solution, the Triathlon Knee System. Should Last 15 Years. The porous femoral component (that is, the part of the replacement that covers the head of the femur, the bone that goes from the pelvis to the knee) is associated with a high rate of failure. Data has shown that up to 25% of patients have anterior knee pain. I was really excited as he doesn't cut the quads making surgery less invasive and the recovery time promised to be quicker and with less pain. Zimmer Knee Implant Injuries New York Failed Implant Product Liability Lawyers Representing Victims of Persona & NexGen Knee Failures. The company issued a voluntary recall for the prosthetics. of the NexGen Complete Knee Solution LPS Femoral Components. came onto the market with a family of knee replacement devices known as the NexGen Complete Knee Solution system in the 90's. The NexGen LPS-Flex GSF Femoral Component was also part of the series of Zimmer NexGen knee recalls. Search Search. Zimmer Knee Replacement While a Zimmer knee implant recall has not yet been issued, the NexGen CR-Flex has been associated with a higher-than-expected failure rate, according to new research. Medical device manufacturer Zimmer issued a recall of its Persona Trabecular Metal Tibial knee replacement in March, 2015. I research it and I could not believe that the knee was on recall. health regulators that is recalling a surgical instrument used in implanting its NexGen replacement knee product. ZIMMER KNEE RECALL: Zimmer Recalls NexGen Knee Replacement Component Due to Risk of Failure - Zimmer NexGen Knee Failure Rate May Be Unusually High Lawyers Offer Free Zimmer NexGen Knee Case Review Zimmer, Inc. With little to no FDA review they were rushed to market with the hopes of offering previously undreamed-of levels of mobility to the thousands of people suffering from decreased range of motion and chronic pain due to deterioration of their knees. Additionally, Zimmer documented the production of the NexGen LPS femoral and tibial components implanted in. Stryker Orthopaedics has initiated a recall for specific lots and sizes of the Femoral Head products manufactured by the company as a component in hip implants in total hip replacement surgeries. My wife had zimmer knee replacement 3 years ago and failed knees on sept 23/2009, and it needed to be replaced again with Zimmer lcck. 2001, had Zimmer NexGen knee surgery. The company also recalled its Persona Total Knee Replacement in May 2019. Recipient's. is recalling 41, 180 stemmed tibial components of the NexGen Complete Knee Solution system. Kurtz titled “Patient-Specific Knee Replacement Implants Preserve Bone and Decrease Blood Loss & Swelling” presented at the 2013 BASK Annual Meeting, comparing 66 iTotal patients with 66 patients receiving one off-the-shelf implant brand (Zimmer NexGen), thickness of the femoral (distal and posterior medial/lateral), and. See who you know at Inserra l Kelley l Sewell, Injury Attorneys, leverage your professional. Zimmer Inc. Zimmer NexGen Knee Replacement Lawsuit; “Vehicle recalls and defects are not only an inconvenience but can also lead to serious accidents and injuries. 2019 products sale. Talking to my OS and he told me he prefers a minimally invasive technique that he has been practicing for 4 years. com The Zimmen [email protected] Knee Replacement System is the world's most clinically proven knee system Zimmer is a pioneer and leader in providing knee replacement solutions that alleviate pain, restore mobility and improve the quality of life for patients. Social; Share on Social Media. Zimmer Biomet has voluntarily recalled multiple devices over the years (Biomet recalled 25; Zimmer recalled 104). The FDA issues a Class II Recall when a product can cause temporary or medically reversible adverse health consequences. I you believe you have taken all the proper steps to care for your implant and the failure is due to a faulty prosthesis, you should contact a Seattle knee recall attorney. Complications With Knee Implants. shown procedures. As a result of defective designs, individuals throughout the United States may have been exposed to an increased risk of loosening or early failure, often resulting in the need for knee revision surgery. Profemur Recall Smith & Nephew Knee Replacement St. Loose parts in a knee replacement cause pain, discomfort and can result in revision surgery which can be costly, painful and may not fully fix the original problem. Zimmer Hip & Knee Replacement Lawsuits Speak to Our Corpus Christi Defective Medical Device Lawyers Today. A DePuy Attune Knee, which has a five-year failure rate of nearly 68 percent, is also the target of several investigations. The NexGen knee system by Zimmer is a comprehensive suite of implants for primary and revision knee replacement. In 2017, the hip replacement market was the largest segment of the overall Japanese orthopedic large joint device market. Zimmer knee replacement lawsuits are serious matters and you need a top product liability attorney on your side!. [2] These cases have been consolidated into a Multi-District Litigation (MDL). OVER 40,000 ZIMMER NEXGEN KNEE TIBIAL COMPONENTS RECALLED (Orthopedics This Week) Zimmer Holdings, Inc. If you or a loved one has suffered injuries by another dangerous drug or medical device, we are always available to answer your legal questions for free. manufactures knee replacement devices that are approved by the Federal Drug Administration (FDA) for patients with severe knee pain and disability due. Our team of attorneys are currently answering questions for individuals suffering from complications related to their Zimmer knee implants. The Zimmer NexGen knee replacement has been linked to a number of problems, including significant pain, loosening of the knee implant and implant failure requiring additional surgeries. In 2010, Zimmer issued recalls for multiple knee components in its NexGen Knee Replacement system. As we’ve reported previously, Zimmer NexGen LPS knee components were recalled last September. I suffered 3 years with the Zimmer NexGen LPS FlexKnee in me. Please note: At this time, the dangerous drug attorneys at Searcy Denney are not accepting cases for injuries from the Zimmer Biomet Shoulder device. NEXGEN LCCK ARTICULAR SURFACEKNEE PROSTHESIS It is reported that the patient underwent bi-lateral knee replacement in 2004. The Zimmer knee recalls in 2010 informed the public of potential problems linked to the NexGen product line, and in turn warned affected patients that their knee complications may not be normal, run-of-the-mill side effects. Zimmer Biomet Shoulder Injury Lawsuit. CSTi porous coating provides potential for optimal ingrowth fixation. The Persona knee implant is the newest in Zimmer’s line of knee replacement products. Zimmer has been forced to recall its knee devices before, and has set aside a considerable sum to reimburse patients for undergoing additional surgeries. If you have been injured by one of the Zimmer knee replacements and want to join the lawsuit call our dangerous surgical device team today for a zimmer NexGen knee replacement lawsuit to be filed for. Zimmer’s NexGen Complete Knee Solutions for knee replacement was recalled many years ago. Zimmer said the threads on the NexGen Complete Knee Solution Tibial Component. It can be performed as a total or partial knee replacement and generally consists of the replacement of damaged or diseased joint surfaces of the knee with metal or plastic components. Casini, of Granger, for a faulty knee replacement product. As a follow-up of the NexGen TKR, an improved design has recently been introduced by Zimmer: The Persona. However, new research regarding Zimmer knee implant failure of the NexGen CR-Flex was presented at a March 2010 conference among orthopedic surgeons. Your Email. It was in 1968 that Zimmer entered the knee implant market. Zimmer has written to surgeons who have implanted NexGen CR Complete Knee Systems, providing further information about the above issue. The manufacturer, Zimmer, says its recall is voluntary. Zimmer NexGen LPS-Flex Mobile and LPS Mobile Bearing Knees— A mobile bearing option offered that allows for greater motion and flex. Zimmer Knee Replacement Law Firm. The NexGen knee system by Zimmer is a comprehensive suite of implants for primary and revision knee replacement. In a study by W. Zimmer NexGen Knee FDA Recalls Issued to Zimmer Inc. The Class II recall began on Feb. Despite Zimmer's claims that its NexGen Knee Replacement products, such as the NexGen CR, are the best performing of all major knee replacement systems, said has unfortunately received quite a bit of public scrutiny, due to serious complications associated with its use, such as: Loosening or fracture of the implant components. This Zimmer NexGen recall is only for a specific component piece, however some research has revealed a higher than acceptable failure rate involving the Zimmer knee and some doctors have expressed their opinion. I was really excited as he doesn't cut the quads making surgery less invasive and the recovery time promised to be quicker and with less pain. Zimmer NexGen MIS Tibial Component Recall. One of the most recent was in 2017 for more than 28,000 joint components. Smith & Nephew is one of the major players in the orthopedic devices and implants market. A complete selection of components, sizes and fixation options lets you design the right combination for optimal joint reconstruction and stability. Zimmer knee replacement lawsuits are serious matters and you need a top product liability attorney on your side!. In 1997 the NexGen Legacy posterior-stabilized (LPS) prosthesis (Zimmer, Warsaw, IN, USA) was introduced as an evolution of the Insall-Burstein II PS prosthesis (Zimmer). The role of metal allergy, including nickel, in problems occurring with knee replacements and other metal prostheses is a constantly evolving area. There has already been a recall of related to a part of the knee. On September 13, 2010 Zimmer, Inc. Zimmer NexGen Knee FDA Recalls Issued to Zimmer Inc. CSTi porous coating provides potential for optimal ingrowth fixation. Would love nothing more than to get off the bike and not have to stand there for a few minutes holding the bike for support afraid that my knee is going to go out again. Potential Problems With Knee and Hip Implants. This product is known as the Zimmer Durom Cup. Smith & Nephew is one of the major players in the orthopedic devices and implants market. Thousands have been affected. The first product was a total knee unit. Zimmer has written to surgeons who have implanted NexGen CR Complete Knee Systems, providing further information about the above issue. Patients are Demanding Justice. Zimmer offers surgeons a comprehensive suite of innovative and unique knee implants, instruments, and related biologics. The Zimmer NexGen knee replacement system has been associated with a number of adverse side effects that may require painful revision surgery. More than 11,000 units were affected by the recall, which covered all sizes and lots of the devices. Social; Share on Social Media. Recently, there have been increasing concerns specifically about some knee replacement products made by the pharmaceutical company. Many of the Zimmer knee replacement products, including the LPS-Flex Knee, soon began to cause complications. The following hip implant models have. ⭐️⭐️⭐️⭐️⭐️@View products #Click Shop for Low Price REMINGTON 870/1100/11 87 SHOTGUN MAGAZINE EXTENSION TUBES CARLSONS. Zimmer Holdings Inc. Knee replacement (also known as joint arthroplasty) surgery is a pretty common medical procedure which has increased quite a bit in the last few years. A DePuy Attune Knee, which has a five-year failure rate of nearly 68 percent, is also the target of several investigations. However, that same Australian data shows that the Zimmer NexGen LPS has the second highest revision rate of the 20 knee replacement devices listed -- nearly 60% higher than the average. Two prominent Chicago orthopaedic surgeons are calling for the recall of Zimmer's NexGen CR-Flex Knee replacement devices. More than one in three 1 knee joint replacements implanted around the world is a Zimmer Biomet product, making us a trusted source for quality knee replacement products. One study has shown that more than 9 percent of people receiving NexGen knee replacements have needed revision surgery to address the problem within two years of the initial implant procedure. It is chosen by more surgeons for their patients, every day, than any other knee replacement system in the world. Persona Trabecular Plate Loosening. Data has shown that up to 25% of patients have anterior knee pain. Consult A Lawyer on Legal Issues If you or a loved one have suffered an injury due to a defective Zimmer ® knee implant, call or e-mail for a free consultation. Zimmer Holdings, Inc. The Persona knee implant is the newest in Zimmer’s line of knee replacement products. advertised its NexGen knee replacement products as a way to reclaim aspects of life. On the whole, the company continues to defend its Zimmer NexGen knee as a successful knee replacement option. It was believed that this device was the best option for women due to superior fitting parts resulting in increased stability. Discuss types of designs and the brand names from major device companies such as DePuy, Smith and Nephew, Stryker, Zimmer-Biomet. 29, 2012 until Jan. All sizes and lots of the affected devices will be removed from the market and will no longer be distributed. Zimmer NexGen Knee Replacement system was intended to increase range of motion over other devices on the market but several of the Next Generation devices have been the subject of multiple lawsuits and resulted in a high rate of revision surgery. As with all new medical technologies, the Zimmer NexGen knee replacements were meant to revolutionize the knee replacement industry. He told me that my knee was not on recall. of the NexGen Complete Knee Solution LPS Femoral Components. Additionally, the company added to its portfolio the Kinective Technology for hip replacement and Fitmore Hip stem, which received FDA approval in March. The NexGen LPS-Flex GSF Femoral Component was also part of the series of Zimmer NexGen knee recalls. Plaintiffs in this multidistrict litigation proceeding (MDL) are individuals whose native knees were replaced by Zimmer NexGen Flex knee implants during total knee replacement (TKR) surgery. Unfortunately, beginning in 2010, the FDA began issuing recalls for components of the NexGen knee replacement system. ZIMMER KNEE RECALL: Zimmer Recalls NexGen Knee Replacement Component Due to Risk of Failure - Zimmer NexGen Knee Failure Rate May Be Unusually High Lawyers Offer Free Zimmer NexGen Knee Case Review Zimmer, Inc. is an Indiana-based medical device manufacturer that has recently come under fire for defects in their NexGen Knee Implants. Since 2003, more than 150,000 Zimmer NexGen Flex-Knee implants have been sold. received a Zimmer knee replacement in 2009 and was forced to undergo revision surgery two Zimmer Nexgen Knee Implant Products. Zimmer Holdings is an Indiana-based orthopedics company involved in providing hip and knee solutions including joint and skeletal replacement systems and surgical tools as well as biologics designed to assist in joint replacement surgeries. The Recall of the Zimmer Persona Knee Replacement System Establishes a Pattern. According to an FDA Enforcement Report for the week of July 9, 2014, the company is initiating a. Zimmer, Inc. And for many, these problems are later explained by a knee replacement recall. However, new research regarding Zimmer knee implant failure of the NexGen CR-Flex was presented at a March 2010 conference among orthopedic surgeons. Knee problems can be debilitating. have received Zimmer implants. More than 11,000 units were affected by the recall, which covered all sizes and lots of the devices. There has not been a general recall of Zimmer knee products. Overview of the most common implants for total hip and total knee arthroplasty. Patients are Demanding Justice. Talking to my OS and he told me he prefers a minimally invasive technique that he has been practicing for 4 years. Enquire Now The class action will seek compensation for individuals that have suffered complications with the device since their hip replacement. Every Oxford® Partial Knee now comes with the only Lifetime Partial Knee Implant Replacement Warranty † in the U. Consult A Lawyer on Legal Issues If you or a loved one have suffered an injury due to a defective Zimmer ® knee implant, call or e-mail for a free consultation. Two prominent surgeons in Chicago have called for the device’s recall because of the high failure rate. Senator Chuck Grassley has also inquired into the reliability of the products Zimmer continues to put on the market. On the whole, the company continues to defend its Zimmer NexGen knee as a successful knee replacement option. 's NexGen CR-Flex knee implant is one such brand that may be defective based on studies by two Chicago surgeons. The Strom Law Firm is now investigating and evaluating Zimmer NexGen Knee Replacement Lawsuits. For example, the manufacturer of the Zimmer Nexgen artificial knee has recently recalled nearly 50,000 units because of manufacturing defects that can lead to infection, bone loss, and dislocation. The problems with the knee implants include: Failure of the implant; Need for revision surgery; Loosening of the. The Zimmer NexGen Knee Implant was advertised as a product designed to accommodate resumption of high levels of activity. This paper is an effort to identify the innovators who contributed to the development of today's condylar total knee prostheses and the surgical techniques used to insert them. In 2010, the FDA issued a recall for over 68,000 Zimmer NexGen devices already implanted, indicating potential serious health problems associated with the knee system. Zimmer offers surgeons a comprehensive suite of innovative and unique knee implants, instruments, and related biologics. Several components of the Zimmer NexGen replacement line of products have been subject to FDA recall. Some knee replacement systems might cause more harm than good because of product defects. As argued in the Zimmer NexGen high-flex knee replacement cases, the Zimmer NexGen high-flex knee implant complications may include: Knee complication and knee pain. Zimmer said the threads on the NexGen Complete Knee Solution Tibial Component. The company also recalled its Persona Total Knee Replacement in May 2019. The Zimmer NexGen MIS Tibial Component is used to replace the patient’s tibia, or. Zimmer has had a rough year on many fronts, not the least of which is the ever increasing number of lawsuits building against its knee and hip replacements. Several different components used as part of the Zimmer NexGen Flex-Knee replacement system have been associated with increased risk of complications, including pain, swelling, loosening of component parts, and the need for follow-up/revision surgery. Zimmer touts the Persona implant as improving the technology used in its NexGen product line, although that claim is still being studied. Zimmer NexGen Knee Replacement Lawsuit. Zimmer NexGen Los Angeles Zimmer NexGen Defects Attorneys. Proner & Proner is a national law firm representing people injured by defective medical devices such as hip and knee replacements, including Zimmer knee replacement devices. Several components of the Zimmer NexGen replacement line of products have been subject to FDA recall. The specific problem involve a component that is attached to the thighbone without any cement to keep it in place. This product is known as the Zimmer Durom Cup. has recalled thousands of components from the company's NexGen Complete Knee Solution and NexGen CR-Flex Knee Replacement products. The voluntary recall affects 41,180 devices and includes eight sizes (1-8). Several Zimmer Artificial Knee Implants Recalled. Both recalls resulted in pending. Companies should not be able to mislead consumers regarding the durability and expected life of a prosthetic device. The Zimmer NexGen CR-Flex is a synthetic femoral implant which caps the femur (thigh bone) where it connects to the tibia at the knee, without cement. The femoral implant is synthetic device used to cap the femur (the thigh bone) at the point where it connects to the tibia at the knee. The Recall of the Zimmer Persona Knee Replacement System Establishes a Pattern. Consult A Lawyer on Legal Issues If you or a loved one have suffered an injury due to a defective Zimmer ® knee implant, call or e-mail for a free consultation. Since the Zimmer NexGen Knee Replacement System was approved by the FDA in 1994, it is estimated that almost half a million people in the U. The knee replacement system was originally designed to address the unmet needs of patients around the world. Reports of high levels of failure associated with certain types of Zimmer’s® NexGen® Flex Knee replacements [1] have led to hundreds of lawsuits being filed against the device manufacturer alleging the early failure of these knee systems. Zimmer Biomet Knee Replacement Recalls. Let's say an apple represents your knee. Chris Janish, CEO of MTS, commented on the recent announcement, "Just as the NexGen litigation is starting to pick up steam, it is concerning that the Zimmer Persona knee seems to just be the start of yet another knee recall litigation. Proner & Proner is a national law firm representing people injured by defective medical devices such as hip and knee replacements, including Zimmer knee replacement devices. , the maker of artificial joint replacement systems, recently announced the recall of more than 65,000 NexGen MIS tibial knee replacement components…. The announcement from the FDA said that Zimmer was initiating a voluntary recall of the Persona knee implant. Social; Share on Social Media. 's NexGen CR-Flex knee implants. While this device and the High Flex versions have not been recalled, a similar device - NexGen LPS - was taken off the market in 2010. With little to no FDA review they were rushed to market with the hopes of offering previously undreamed-of levels of mobility to the thousands of people suffering from decreased range of motion and chronic pain due to deterioration of their knees. By: Chris Dixon • October 6, 2011 Zimmer NexGen has recently issued a number of recalls related to Zimmer NexGen knee replacement knee components. Zimmer Knee Replacement Recall. The ASR XL recall was issued in 2010 and the other in 2013. Zimmer Knee Implant Injuries New York Failed Implant Product Liability Lawyers Representing Victims of Persona & NexGen Knee Failures. Complications include pain, swelling, loosening of component parts, and necessary revision surgery. The next time I saw my surgeon, I said how can the Mayo Clinic give me a prostectic knee that is on recall. Patients are Demanding Justice. Zimmer knee replacement systems. Manufacturers may voluntarily recall knee replacements when they discover a problem. Zimmer Manufacturing initiated another sweeping recall on one of its artificial knee implants, because one of the pieces could loosen or fail because of shoddy manufacturing. Knee & hip replacement devices have injured thousands in the U. If you are a recipient of the Zimmer NexGen knee replacement and are questioning its stability, safety, or reliability, you are not alone. of the NexGen Complete Knee Solution LPS Femoral Components. Zimmer NexGen Knee Recall Zimmer Holdings, Inc. This includes the 1995 release of the NexGen Complete Knee Solution System. The Class II recall began on Feb. Discuss types of designs and the brand names from major device companies such as DePuy, Smith and Nephew, Stryker, Zimmer-Biomet. Some Zimmer NexGen knee replacement systems have been linked to a high number of problems, including reports of pain, loosening of the implant and failure of the replacement knee leading to revision s. The Arcos Platform - Comprehensive Solutions that Simplify. The Zimmer NexGen knee replacement has been linked to a number of problems, including significant pain, loosening of the knee implant and implant failure requiring additional surgeries. This component was created and marketed for use in female knee replacement patients. Code Information: All lots. Tibial component implantation uses existing NexGen instrumentation; Many daily activities require flexion beyond 120 degrees. OVER 40,000 ZIMMER NEXGEN KNEE TIBIAL COMPONENTS RECALLED (Orthopedics This Week) Zimmer Holdings, Inc. Berger’s warnings, United States Senator Charles E. The Persona knee implant is the newest in Zimmer's line of knee replacement products. Cutting edge instrumentation, such as the user friendly MIS system and the ream-thru femoral trials, was designed to create the most comprehensive system available. However, that same Australian data shows that the Zimmer NexGen LPS has the second highest revision rate of the 20 knee replacement devices listed -- nearly 60% higher than the average. Food and Drug Administration can order a recall. Although Zimmer ignored Dr. Specific models associatd with dangerous side effects include the Zimmer NexGen CR-Flex, CR-Flex Porous Zimmer NexGen, and the MIS Zimmer NexGen LPS. Our Zimmer Knee Implant attorneys are available 24/7 to help you. Zimmer has been developing total knee replacement systems since 1968. is one of the leading orthopedic device makers in the country and their products leading up to 2017 heavily dominated the market in close competition with DePuy and B. Several Zimmer Artificial Knee Implants Recalled.