List of recalled knee replacements

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August undefined, 2024

WebReasons for knee replacement device recalls. To date, there have been 125 knee replacement device recalls since 2003. These include a Class I recall for the Stryker ShapeMatch Cutting Guide device, which was acknowledged by Stryker to have problems and surgeons had been advised not to use it. Web9 aug. 2024 · If you wish to find information on a recall, or a correction or removal action that has not yet been classified, you can search the Medical Device Recalls Database. Please note that the FDA lists ...

Product Recalls and Alerts - GOV.UK

WebThe Attune Knee System was introduced by DePuy Synthes as a result of the largest research and development project in the company’s history, and was designed to improve function through mobility and stability of the … Web29 sep. 2024 · The most common type is the total knee replacement, which replaces the entire joint with artificial components. Other types of DePuy knee replacements include … philip flybring

Medical Device Recalls FDA

WebLargest Knee Recalls Since 2015 January 2016 Device: Zimmer NexGen Complete Knee Solution Cruciate Retaining (Cr)Flex Femoral Components Number Recall: 42,064 … Web21 sep. 2024 · Almost all of the major companies that manufacture knee replacements implants have had at least one recall, including: Biomet; Smith & Nephew; DePuy; … WebZimmer has also issued multiple recalls in the last 5 years. 2010 – Zimmer recalled roughly 70,000 of it MIS Tibial. 2014 – Zimmer recalled 40,000 NexGen Knee implants. 2015 – Zimmer recalled over 11,000 Persona Knee implants. The attorneys at Anvil legal Group have experience representing plaintiffs in product liability lawsuits. philip flynn

Knee Replacement - Implants Subject to Recalls, …

Exactech Recall Information Surgeons and Patients

Web27 aug. 2010 · Aug. 26, 2010. More than two years after the Food and Drug Administration began receiving complaints about the failure of a hip replacement implant made by the DePuy Orthopaedics unit of Johnson ... WebFebruary 15, 2024 — Exactech has recalled about 140,000 knee and ankle replacements that were implanted in patients in the U.S. since 2004 because they can wear out early. The implants were recalled because they can fail prematurely, crack or fracture, cause bone loss, or other problems that require surgery. philip flynn associated bankWeb7 apr. 2024 · The PAS 7100:2024 on Product Recall and Other Corrective Actions: Code of Practice is also available: Access PAS 7100:2024 – BSI website. If you are an MSA and need to add a product to the list ... philip fluorescent tube

"Web4 apr. 2024 · At the time of the Zimmer voluntary recall, more than 11,000 Zimmer Persona knee replacement devices had already been implanted. A Class 2 recall is assigned when it is discovered that a medical device could cause reversible or temporary health threats. " - List of recalled knee replacements

List of recalled knee replacements

Exactech Recall Information Surgeons and Patients

WebA knee replacement is really just a RESURFACING of) the end of the femur (thigh bone), b) the top of the tibia (shin bone) and c) the undersurface of the patella (knee cap). Contrary to popular perception, we remove just a thin layer of bone, leaving the rest of the bone and ligaments around the knee undisturbed. Check out the picture below. Web23 mrt. 2024 · Metal-on-metal hip replacements used through the mid-2000s and early 2010s can cause permanent physical damage to patients. Studies show that metal debris from this type of hip replacement can destroy muscle, bone, and tissue around the implant. Even worse, the metal debris can travel through the body and cause organ damage, …

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WebJohnson & Johnson knee replacement systems have had numerous problems that have resulted in the recall of the product Monday, July 31, 2024 - When you earn close to 100 billion dollars per year, year in and year out, settling a lawsuit for one or two billion dollars is merely a cost of doing business. Web28 mrt. 2024 · Which Exactech Knee Replacement are Recalled? The recalled Exactech Knee replacements include: OPTETRAK Comprehensive Knee System; TRULIANT …

WebKnee replacement recalls have been issued because of loosening, early wear or faulty packaging. Nearly 1,000 implant parts used in knee surgeries have been affected by DePuy, Zimmer-Biomet and Stryker knee replacement recalls. Lawsuits blame manufacturers … Web17 feb. 2012 · In recent years, a number of Smith & Nephew recalls have been issued for different components used in the company’s knee replacement systems. Nearly 40,000 Journey Uni Tibial Baseplates were...

WebA recall has been issued for Stryker ShapeMatch Cutting Guides, which were used with Stryker Triathlon knee replacements to help surgeons plan out and mark bones before surgery. A number of... Web16 jan. 2012 · Smith & Nephew Journey-Deuce Uni Tibial Baseplates: Recalled in 2010 (40,000 units recalled) The baseplate (circled in red) rests on the tibia (the bottom leg bone), and attaches to the knee replacement hardware on the femur (the top leg bone). Because these baseplates are breaking, the entire knee replacement can become …

Web12 mrt. 2024 · The knee replacement devices that have currently been recalled are the Exactech Optetrak, Logic, and Truliant knee replacement systems. These devices were recalled due to the presence of a polyethylene defect found in …

Web13 mei 2024 · To date, the recall covers approximately 140,000 knee and ankle replacements manufactured since 2004. It includes versions of Exactech’s OPTETRAK … philip flynt cpaWeb5 aug. 2014 · Recalled knee implants and components reported to the FDA up to May of 2013: Biomet : 75 recalls (all class II). Recalled models include the Vanguard PS Open Box Femoral Component (2007, mislabeling); … philip fluorescent light bulbsWeb18 okt. 2024 · In one of the largest knee implant settlements, Sulzer Medica agreed to pay $1 billion to settle roughly 4,000 lawsuits over its hip and knee implants in 2002. The settlement averaged $200,000 per patient. In 2000, the Swiss company recalled thousands of hip implants that had been tainted with a lubricant. philip f. maritzWebHernia Mesh Recall Hip Replacement Recalls Knee Replacement Recalls DePuy Knee Replacement L-Citrulline Recalls Power Morcellator Recalls Risperdal and Invega … philip flynn odWeb1 aug. 2024 · Oxidized zirconium was introduced as an alternative bearing surface to decrease polyethylene wear and reduce aseptic mechanical failure of hip and knee arthroplasties. Oxidized zirconium combines the strength of a metal with wear properties of ceramic, proposing increased survivorship of implant components, and possible … philip f margoWeb13 mei 2024 · Plaintiffs continue to file claims post-recall. In March 2024, a plaintiff in the Southern District of New York filed a complaint against Exactech. The plaintiff alleged that the OPTETRAK Logic total knee replacement systems the plaintiff received in 2013 and 2015 were defective. The patient suffered “pain, swelling, instability, and bone ... philip f moore murrieta californiaWebThe NexGen Knee System also offers solutions for Revision Knee Arthroplasty with the NexGen Legacy ® Constrained Condylar Knee (LCCK) and NexGen Rotating Hinge (RH) Knee. Learn More NexGen MIS LPS-Flex Mobile Implant System NexGen LPS Fixed Bearing Knee NexGen LPS-Flex Mobile and LPS-Mobile Bearing Knees (U.S Version) philip flynn obituary