zimmer biomet knee replacement recall

Zimmer knee replacement litigation. Some of the problems that patients reported with their Zimmer Persona knee system included aseptic loosening of the joints, premature failure of the knee replacement . Class 1 Device Recall LPS Diaphyseal Sleeves Retrieved from, U.S. Food and Drug Administration. iTotal CR (2015) iDuo (2015) iTotal PS systems (2015) Get to know Zimmer Biomets leadership team. Customers who have questions about this recall should contact their Zimmer Biomet representative or customer service by email at Medtech-CHT@zimmerbiomet.com or by phone at (574) 373-5097. NexGen is the second most popular knee replacement product. Retrieved from, Meier, B. For more information, visit our partners page. "logo": { The Zimmer knee device that was named in the recall was the Persona trabecular metal tibial plate. Sorry there is a continuing error in our system. Manufacturers issue knee replacement recalls for several reasons. All content herein is protected by copyright, trademarks and other Many of these cases had to do with premature loosening of the joint replacement device. Zimmer Biomet offers a wide variety of solutions that address Our writers are members of professional associations, including American Medical Writers Association, American Bar Association, The Alliance of Professional Health Advocates and International Society for Medical Publication Professionals. Please do not include any confidential or sensitive information in a contact form, text message, or voicemail. Testing Positive for COVID-19: It Felt Like I Had a Compression Belt Around My Chest, COVID-19: A Consumers Guide to the Coronavirus, Trial Attorney and Pharmaceutical Litigation Expert, Zantac Cancer Lawsuits Dismissed by Federal Judge, Erika Sward of American Lung Association Reveals the Dangers of Vaping and IQOS. And lawyers report new cases claiming injuries from the DePuy Synthes Attune Knee implant and the first-generation Smith & Nephew Journey BCS knee system. A federal judge granted a motion for stay of 16 cases in MDL 2391 through November 2020. Over the course of 24 months prior to issuing the notification letters, Exactech made observations that the GXL polyethylene liners used as part of its hip replacement systems had risks of wear that could cause osteolysis or bone deterioration. Privacy Policy | It has had 377 separate recalls since 2003, and, again, this number reflects separate brands being recalled, not the number of individual pieces that were pulled off the market. Medical Device Recalls (Accessed May 9, 2018). Join our newsletter to stay up to date on dangerous drugs and devices, keep up on lawsuit and settlement news, learn about FDA recalls, and more. challenges that are often encountered during revision kneearthroplasty. For more than 40 years, we've helped personal injury victims who have been hurt in accidents or by defective medical devices such as . Retrieved from, U.S. Food and Drug Administration. With total knee replacement, the entire surface has to be removed. (2019, April 9). The Oxford Partial Knee is intended for use in individuals with No significant case developments are expected in the meantime. Learn more about the cookies we use. Product Usage: This device is designed to hold the patient s knee in the selected position during surgery. . had risks of wear that could cause osteolysis or bone deterioration. E-mail any problems with this form to: Lost Wages and Loss of Future Income: Victims defective medical implants have a right to recovery for lost wages as well as loss of future income. (2010, June 20). The metal is titanium, which is a strong, light metal that is resistant to corrosion. Potential risks Most notably, on February 22nd, Zimmer Biomet was issued a total of 5 recall orders pertaining to their Oxford product line due to potential alumina inclusion in the finished product that could lead to cracking and separation. Wright sold its hip and knee division to Corin Orthopaedics in 2016 for a reported $290 million. Top Class Actions is a legal news source Knee Replacement Device Recalls. Sorry there was an error. Class 2 Device Recall Zimmer Biomet. Helped more than 12,000 people find legal help. Some patients, however, continue to suffer significantly even after getting medications injected into the joint. page, Hospital Negligence Compensation Solicitors, Go to the Residential Conveyancing "@type": "ImageObject", Wright Conserve Hip Implants Board-certified physicians medically review Drugwatch content to ensure its accuracy and quality. drug injury lawsuits and product liability lawsuits. Biomet UK issued a voluntary field safety corrective action; analysis identified a world wide occurrence of 0.12% of . All Rights Reserved. Zimmer Biomet opted for the opposite strategy, shedding its spine and dental businesses and creating ZimViewho should appear on next year's list. Zimmer Biomet, the American medical device manufacturer has issued a voluntary recall of more than 10,000 of its 'NexGen' knee replacements. Recall # Z-2156-2020. [gravityform id="805" title="false" description="false" ajax="true" field_values="l=US"],

Our team includes experienced medical writers, award-winning journalists, researchers and certified medical and legal experts. Two bones stretch from the ankle to the knee known as fibula and tibia respectively. We use an experienced team of independent biomedical and medical experts to give evidence on that issue. Stryker voluntarily recalled its ShapeMatch Cutting Guides after patients reported injuries. page, Sales and Purchases of Commercial Property, Go to the Employment Law & HR settlement administrator or your attorney for any updates regarding There have been 125 Stryker knee replacement recalls since 2003. Zimmer Biomet has issued at least 355 knee replacement-related recalls since 2003. With the growing number of revision surgeries among patients, the US Food and Drug Administration issued a recall notice to Zimmer Holdings Inc. to withdraw the faulty knee replacement device from the market. Knee replacement lawsuits frequently claim the devices loosened or became so unstable they had to be replaced. The Alvarado Knee Holder includes a Base Plate assembly with two rows of slotted hooks. One of the most common reasons for undergoing knee replacement with a Zimmer Persona knee system, prior to the recall, was a diagnosis of knee osteoarthritis. The follow-up review of the NexGen Complete Knee System was conducted by David Keohane, an Orthopaedic . "url": "https://www.ringroselaw.co.uk/team/richard-teare/" The common symptoms of device failure that a patient may experience are. To date, Zimmer Biomet are the only knee replacement implants manufacturer that has experienced mass litigation relating to this type of medical device, with 1,700 individual lawsuits documented up to 2019 and many thousands of units recalled. We tell you about cash you can claim every week! Knee Replacement Warnings and Recalls. You can change these settings at any time. Retrieved from, DePuy Synthes. It is the latter one that is the larger of the two and is responsible greatly for an individuals movements and mobility. fixation, constraint, soft tissue and boney defect management According to new reports, the Zimmer NexGen CR-Flex knee replacements can fail at an unexpectedly high rate within a few years of surgery. Patients' X-rays of their Zimmer Persona knee implants often showed gaps between the tibial plate device and their bones. counseling information, see the package insert and information on this Knee osteoarthritis is a condition that can impact a patients every move: climbing stairs, walking or even lying down and sitting. }, Contracted with The Legal Aid Agency Copyright Ringrose Law 2013 VAT No.127768439 Authorised and Regulated by the Solicitors Regulation Authority of England and Wales 0058125 The Solicitors Regulation Authoritys rules can be accessed at rules.sra.org.uk, This site is protected by reCAPTCHA and the Google, Zimmer Biomet NexGen Recall 10,000 Faulty Knee Replacements. He answered all questions and returned all calls and texts. Like DePuy, Zimmer Biomet had a big recall in 2017. We strive to alleviate pain and improve the quality of life for people around the world. We use cookies to improve functionality and performance, enhance user experience, and provide tailored content. PRN is a nationally recognized leader in providing independent medical reviews. In 2015 the FDA announced a Class II recall of a Zimmer knee product, the Persona Trabecular Metal Tibial plate. The most common reason for knee replacement implant recall is reported adverse events linked to a manufacturing defect of an implant, such as: Premature implant failure or loosening. Any unauthorized or illegal use, copying or dissemination will be prosecuted. It also allegedly led to revision surgeries. However, patients began to develop complications that lead to pain, suffering, and often revision surgeries. *4-5 And now, Zimmer Biomet offers the only Partial Knee Lifetime Implant Replacement Warranty.. Zimmer Biomet, Inc. - the manufacturer of the Zimmer Persona Knee system - quietly recalled various components used to facilitate the installation of joint replacement implants. In September, 2010, the FDA categorized this as a Class II action as a response to nearly 114 MDRs or medical device reportings. It was formally withdrawn from the . 1 Zimmer Biomet offers surgeons Total Knee Systems that are designed Seemlessly connect, products, services and technologies to elevate An unspecified number of Zimmer Biomet implants were recalled in 2020 when samples were found to exceed the FDA-adopted standard for endotoxin levels.

Review our editorial policy to learn more about our process for producing accurate, current and balanced content. Get to know Zimmer Biomet's leadership team. Zimmer Biomet Partial Knee Replacement. It is not a substitute for professional medical advice, diagnosis or treatment. The company took on its present form with the merger of Zimmer and Biomet in 2015. This is classified as early failure and more often than not, requires revision surgery. The NexGen device has been found to loosen without any underlying cause in a process known as aseptic loosening (failure without infection). Unfortunately, many artificial joint recipients are finding that knee replacement surgery can cause more harm than good. }, Failing to do so may result in you not getting signed up as a client or getting you dropped as a client. A vocational expert will determine the value of lost wages by calculating the days . These gaps are an example of poor seating or movement . . Retrieved from, Gann, C. (2012, February 10). Drugwatch's trusted legal partners support the organization's mission to keep people safe from dangerous drugs and medical devices. These can be as simple as faulty packaging on knee replacement parts.

AAHKS November 3-6, 2022. Plaintiffs argue defective and dangerous NexGen knee components are the result of a failure to perform sufficient . Date: January 28 th, 2017: Reason for Recall: The operation itself is invasive and carries risks associated with anaesthetic, infection, nerve and tissue damage and poor recovery. Thus the calculation of would be 400 days plus 20 X 365 days = 7,700 days multiplied by $500 equals $3,850,000. Biomet was a successful Indiana medical device company that was snapped up by Zimmer in 2014 for $13.4 billion. Biomet . Quickly find individual products and their details. "dateModified": "2022-12-14" Zimmer decided to recall a component of the Persona knee replacement system the Persona Trabecular Metal Tibial Plate after it became aware that the product was loosening after surgical implantation. I found information that was very helpful, that her psychiatrist never told her.". If you or a loved one has been affected by a recall, it is important to seek legal counsel to ensure your rights are protected. Our lawyers at the Logue Law Group have the reputation of providing impartial and exclusive attention to each client. This was a Class 2 device recall that was initially posted in March of 2015. Sign up for our free newsletter. Wright Medical announced four knee replacement recalls since 2003. Zimmer Biomet. Is There a Recall on Zimmer Knee Replacements? In Re Zimmer NexGen Knee Implant Products Liability Litigation, MDL No. Retrieved from, U.S. Food and Drug Administration. "image": "https://575367.smushcdn.com/1986401/wp-content/uploads/knee-replacement-recall-560x280.webp?lossy=1&strip=1&webp=1", Logue Law Group has helped many clients who claimed to have undergone revision surgeries and extensive side effects because of the implantable NexGen MIS device. . for full prescribing and risk information, please call 1-800-348-2759, press 4 for 411 Technical Support., ROSA Robotics Certification Training Scottsdale AZ 01.13-14.23, Anterior Hip Advanced Primary BioSkills Course with Technology Solutions Dinner Scottsdale 02.02-03.23, ROSA Robotics Certification Training Scottsdale AZ 02.3-4.23, Zimmer Biomet Announces Quarterly Dividend for Fourth Quarter of 2022, Zimmer Biomet to Present at Goldman Sachs CEOs Unscripted Conference and 41st Annual J.P. Morgan Healthcare Conference, Zimmer Biomet to Present at the 34th Annual Piper Sandler Healthcare Conference. Oxford Partial Knee is not indicated for use in the lateral Dislocation (the device does not lock properly after implant), Swelling and inflammation at the site of surgery, Shooting pain along the leg where replacement surgery took place, It can cause serious difficulty in standing up and walking around by oneself, Loosening of the NexGen MIS Tibial component can cause the device to slip out of the socket. We will direct you to one of our trusted legal partners for a free case review. (2018, January 17). knee replacement procedure. The Zimmer Persona Knee recall affected nearly 12,000 components that may have been implanted in patients who were placed at risk of early device failure. Please note: Top Class Actions is not a settlement administrator or law firm. The NexGen MIS Tibial device is implanted in the patient during the knee replacement surgery through a small incision. systems, bicruciate preserving arthroplasty systems and revision knee The structure of this component is such that it was easier both for the surgeon and the patient to tackle with it. Two other companies combined for only 19 recalls between them. But critics argue that the FDA approval process does not do enough to keep unsafe devices off the market. Knee replacement recalls have been issued because of loosening, early wear or faulty packaging. Smith and Nephew has announced 15 knee replacement-related recalls since 2003. Zimmer Biomet- Knee Product: TMJPM-1510 Microfixation Custom Made Device, Left PM-TMJ Model (01)00841036226534(17)220111(10)735550 . The list of knee replacement recalls for 2017 below consists of only FDA recalls. Zimmer Biomet was a successful Indiana medical device company that was acquired by the company for $13.4 billion in 2014. Head and Brain Injury Compensation Claims, Go to the Domestic Judicial Panel on Multidistrict Litigation. Zimmer Biomet Announces Quarterly Dividend for Fourth Quarter of 2022 December, 15, 2022. Zimmer . Arthrex has issued two recalls related to its iBalance knee replacement line: one for the iBalance Total Knee Arthroplasty System and another for the iBalance Unicondylar Knee Arthroplasty System. Over 28,000 individual joint components were . The ROSAKnee System supports surgeons in performing You must contact the (2017, October 3). It has approximately 40% market share, followed by Stryker (SYK), Johnson & Johnson (JNJ), and Smith & Nephew . A number of knee replacement devices sold by U.S. manufacturers have been recalled by the Food and Drug Administration due to manufacturing defects or high rates of device failure which result in serious injury. . "@type": "NewsArticle", If yes, then Sean Logue is the attorney you want on Attorney Logue represented me well and took care of my legal issues superbly. One of the most recent was in December 2017 for Sigma knee components. Mass Device. Previous Smith & Nephew recalls involved fewer than 100 total units. The plastic is polyethylene, which is a durable plastic that is easy to clean and is not susceptible to infection. Zimmer Biomet is currently named as the defendant in more than 700 lawsuits alleging complications from its NexGen knee replacement implants. , This material is intended for health care professionals. Do Not Sell My Info. Patient. The letter informed customers of the product commingling issue. Click Change Settings if you want to tailor the use of your cookies. is_redirect && ! If the implant was given to a patient prior to the termination date of the recall, problems could still begin to manifest for the patient like pain or plate loosening. However, 350 early failures (within 10 years) have already been reported giving the NexGen implant an unacceptably high failure rate of around 7% with some medical studies suggesting the actual failure rate is higher still as more patients continue to report early failures. Persona OsseoTi is the latest addition to the clinically proven . Class 2 Device Recall Journey BCS Knee System. 91-B(6 . Distribution to any other recipient is prohibited., For product information, including indications, contraindications, Smith & Nephew. page, Medicines and Healthcare Products Regulatory Agency. is_confirmation;var mt = parseInt(jQuery('html').css('margin-top'), 10) + parseInt(jQuery('body').css('margin-top'), 10) + 100;if(is_form){jQuery('#gform_wrapper_805').html(form_content.html());if(form_content.hasClass('gform_validation_error')){jQuery('#gform_wrapper_805').addClass('gform_validation_error');} else {jQuery('#gform_wrapper_805').removeClass('gform_validation_error');}setTimeout( function() { /* delay the scroll by 50 milliseconds to fix a bug in chrome */ jQuery(document).scrollTop(jQuery('#gform_wrapper_805').offset().top - mt); }, 50 );if(window['gformInitDatepicker']) {gformInitDatepicker();}if(window['gformInitPriceFields']) {gformInitPriceFields();}var current_page = jQuery('#gform_source_page_number_805').val();gformInitSpinner( 805, 'https://s40123.pcdn.co/wp-content/plugins/gravityforms/images/spinner.svg' );jQuery(document).trigger('gform_page_loaded', [805, current_page]);window['gf_submitting_805'] = false;}else if(!is_redirect){var confirmation_content = jQuery(this).contents().find('.GF_AJAX_POSTBACK').html();if(!confirmation_content){confirmation_content = contents;}setTimeout(function(){jQuery('#gform_wrapper_805').replaceWith(confirmation_content);jQuery(document).scrollTop(jQuery('#gf_805').offset().top - mt);jQuery(document).trigger('gform_confirmation_loaded', [805]);window['gf_submitting_805'] = false;wp.a11y.speak(jQuery('#gform_confirmation_message_805').text());}, 50);}else{jQuery('#gform_805').append(contents);if(window['gformRedirect']) {gformRedirect();}}jQuery(document).trigger('gform_post_render', [805, current_page]);} );} ); Zimmer Knee Replacement Reviews & Problems. systems that empower you to offer a patient specific approach for each Terms and Conditions. Lawsuits have been filed all over America in an attempt to hold the device's multibillion . DePuy Synthes has issued hundreds of recalls over the years. Zimmer Biomet has more than 45 years of experience in partial knee arthroplasty and currently holds more than 50 percent of the global partial knee market share. A Zimmer knee replacement recall has not yet been issued. } (2017, December). osteoarthritis or avascular necrosis limited to the medial compartment "author": { (2018, March 23). Patient. Zimmer Biomet hip replacement recalls are a serious matter. A Class 2 recall is assigned when it is discovered that a medical device could cause reversible or temporary health threats. The lines between traditional medtech and digital healthcare continue to blur, and a perfect example of this trend is Zimmer Biomet's Persona IQ smart knee implant, which is now FDA cleared. It lets knee replacement makers skip more rigorous tests. and combinations, allowing a patient specific approach to reconstruct (2012, January 11). Studies have shown that 15%-39% of patients who undergo total knee surgery are not satisfied with the outcome. The recalls included nearly 250,000 package and label issues, knee implant parts and tools used in knee replacement surgery from 2014 through 2017 alone. The Ruth Law Team handles many types of medical device and product liability claims. Whilst implant failure is a recognised complication of all joint replacement surgery the average incidence across all products is approximately 2.4%. Drugwatch partners with Physicians Review Network Inc. to enlist specialists. Thus, at this time, the GXL liner has been transitioned entirely out of the US market. Recipients thought a knee replacement would impact and improve their mobility but rather left them suffering from pain, device break down and revision surgeries. Other knee replacement recalls by Zimmer Biomet in 2017 included: Date: January 6 th, 2017: Reason for Recall: Mislabeling of right Oxford Fixed Lateral Bearings as left Bearing: Product(s) Affected: Oxford Fixed Lateral Bearing Size F Right .
Lawsuits blame manufacturers for selling defective devices. Zimmer Inc., based in Warsaw, Ind., was founded more than 80 years ago and is now one . Smith & Nephew - 139 recalls. Alvarado Knee Positioners Recalled by Zimmer Biomet through FDA.
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The devices had higher than expected failure rates. (2017, February 17). compartment or for patients with ligament deficiency. They only have to show their device is substantially equivalent to similar products. facilitate implant positioning intraoperatively.. Zimmer Biomet has faced more than 1,700 lawsuits over its NexGen implant. Knee Replacements Double in 10 Years. Amanda Pedersen | Aug 30, 2021. While Exactech has noted that it is not officially recalling its Connexion GXL hip replacement liners, in letters provided to surgeons and patients in June 2021, the company explained that GXL liners were transitioned out of the US market due to risks of premature wear and possible complications. Manufacturers often rely on the agencys Premarket Notification process. If you have experienced problems following knee replacement surgery or any with any other medical device, contact the Ringrose Law Medical Negligence team. The knee implant attorneys who work with Top Class Actions will contact you if you qualify to let you know if an individual lawsuit or class action lawsuit is best for you. Retrieved from: FDA. As of 2016 they controlled 31% of the market and made $1.8 billion off their hip surgery implants that year. Logue Law Group Team. This article contains incorrect information, This article doesn't have the information I'm looking for, Total Knee Replacement Increases Hip Fracture Risk, FDA Issues Notice of Class 2 Recall for Zimmer Persona Knee Implant, Exactech Transitions GXL Liners Out of the US Market, https://www.fda.gov/medical-devices/medical-device-recalls/what-medical-device-recall, https://abcnews.go.com/blogs/health/2012/02/10/knee-replacements-double-in-10-years-study-says, https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=106058, https://www.nytimes.com/2010/06/20/business/20knee.html, http://www.jpml.uscourts.gov/sites/jpml/files/MDL-2272-Tag-Along-Transfer-03-15.pdf, https://www.theguardian.com/business/2003/sep/18/6, https://www.bfarm.de/SharedDocs/Kundeninfos/EN/11/2018/00143-18_kundeninfo_en.pdf;jsessionid=CD5D3742F6BB4C481804F1AD461D383A.2_cid354?__blob=publicationFile&v=1, https://www.massdevice.com/revision-rates-prompt-recalls-johnson-johnsons-depuy-synthes-zimmer-biomet/, https://journals.sagepub.com/doi/abs/10.1177/02692155221113909, https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=114764, https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=151861, http://www.smith-nephew.com/global/assets/pdf/corporate/smith_nephew_annual_report_2016_interactive.pdf, https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/resCollection_2.cfm?ID=154239&CREATE_DT=2017-03-27, https://www.bizjournals.com/memphis/news/2016/10/24/wright-medical-sells-hip-knee-division.html, https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm, https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=143925, https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=159082, https://www.accessdata.fda.gov/SCRIPTs/cdrh/cfdocs/cfres/res.cfm?id=165170, https://www.mcgartland.com/wp-content/uploads/2018/07/Smith-Nephew-Field-Safety-Notice-Journey-BCS-Knee.pdf, SIGMA HP MBT Non-Keel Punch Knee Instruments, Design flaw that could cause a delay in surgery, Instrument fracturing during surgery and leaving parts of the rods in patients, Attune Knee Tibial Articulation Surface Instruments, Could come off during surgery, leaving a part in device in the patient, Reports of higher revision surgery rates in Australia, Reports of fractures potentially leaving parts in the patient, Could fracture and pieces could be left in the patient, Defective packaging could compromise sterility, Gender Solutions Patello-Femoral Joint System, Spacer blocks do not fit in the alignment tower instrument or handle, Problems with flexion in range-of-motion trials, Zimmer Biomet polyethylene joint components, Persona Trabecular Metal Tibial Plate Knee implants, Stryker Orthopaedics Patella Assembly Instruments, Parts could come apart from an accompanying instrument during surgery, Parts could come apart from the rest of the instrument, MIS Modular Distal Capture Triathlon Instruments, Reports that parts could come apart from the instruments, Packaging issue could affect the shelf life of the devices sterility, Device misalignment could result in knee implants being placed in the wrong position, Higher than normal revision rates because of early component loosening and other problems, Manufacturing defect; it could make the polyethylene insert difficult or impossible to seat during surgery, Legion Hemi Stepped Tibial Screw-On Wedges, Outer metal surface was smooth compared to previous textured components, iBalance(R) UKA, Femoral Cemented, Size 3, Left Medial/Right LATERAL. Please read our disclaimer for more information about our website. Top Class '> As of June 2020, approximately 50 Biomet hip replacement lawsuits were still active in MDL 2391. "@type": "WebPage", There are currently some 1,000 Zimmer knee replacement lawsuits pending in the courts. "name": "Richard Teare", Bench testing reveals that Exactechs new XLE liner does outperform the Connexion GXL liner in both volumetric wear and edge loading assessments.. patient recovery site. Retrieved from, Hodges, A. et al. March 12, 2015- FDA categorized Zimmer Persona Knee recall as "Class II Recall." Zimmer Persona Knee Reviews. Heeding the call of several prominent knee surgeons, the FDA issued a Class II recall of the Zimmer NexGen CR-Flex knee replacement on March 12, 2015. (2017). In serious cases of wear and osteolysis, patients required revision surgery. Some of his qualifications include: Drugwatch.com writers follow rigorous sourcing guidelines and cite only trustworthy sources of information, including peer-reviewed journals, court records, academic organizations, highly regarded nonprofit organizations, government reports and interviews with qualified experts. Failure to place the device in accordance with these instructions could give rise to a medical negligence claim against the surgeon or hospital where surgery was performed. website. Drugwatch is located at: WARSAW, Ind., Nov. 21, 2022 /PRNewswire/ -- Zimmer Biomet Holdings, Inc. (NYSE and SIX: ZBH), a global medical technology leader, today announced U.S. Food and Drug Administration (FDA) 510(k) clearance for the Persona OsseoTi Keel Tibia for cementless knee replacement. Cementless Oxford Partial Knee Unicompartmental Knee Replacement System. After fighting a ticket from hell that cost me my job, thousands in debt from having no job and threatening my present career, Sean Logue stepped in and the case was dismissed. status of any class action settlement claim. "datePublished": "2022-12-12", Memphis Business Journal. Decide which cookies you want to allow.