List of recalled knee replacements

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August undefined, 2024

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... 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.

Knee Replacement Lawsuits Settlements and Verdicts

WebDePuy Knee Replacement Systems. DePuy Synthes, often referred to just as DePuy, is a major subsidiary of Johnson & Johnson. It is one of the largest manufacturers of hip and … 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 … fisher litoměřice

Exactech Joint Replacement Lawsuits 5 Things to Know

WebMedical Device Recalls. This database contains Medical Device Recalls classified since November 2002. Since January 2024, it may also include correction or removal actions initiated by a firm prior to review by the FDA. The status is updated if the FDA identifies a violation and classifies the action as a recall and again when the recall is ... 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. 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... canadian royal purple society williams lake

Knee Replacement Lawsuits Settlements and Verdicts

Medical Device Recalls - Food and Drug Administration

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. WebWhile there have been no reported settlements or verdicts in an Exactech knee and ankle implant case, base awards in recent hip replacement cases fall within the $150K to $300K range. Typically, knee implant cases have a lower compensation value than hip replacement cases but there are no hard-and-fast rules about this. canadian royal bank onlineWebLargest Knee Recalls Since 2015 January 2016 Device: Zimmer NexGen Complete Knee Solution Cruciate Retaining (Cr)Flex Femoral Components Number Recall: 42,064 … canadian royal henley regatta

"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 ... " - List of recalled knee replacements

List of recalled knee replacements

Exactech joint replacement devices with defective packaging

WebYou have several ways to determine if your knee replacement was part of a recall. You could: Speak with your doctor or surgeon. Review the recall database from the U.S. Food & Drug Administration (FDA) Review the manufacturer’s recall database. Typically, surgeons receive warning letters about medical device recalls for products they may have ... Web30 mrt. 2024 · Unicompartmental Knee System (recalled in 2011) – recall was terminated in 2014 by USFDA. Smith & Nephew. Journey Uni Tibial Baseplate (recalled in 2009) – recall was terminated in 2011 by USFDA. Biomet. Vanguard PS Open Box Femoral Component (recalled in 2007) – recall was terminated in 2008 by USFDA.

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Web10 feb. 2024 · A quick search on theFDA Medical Device Recallspage reveals knee replacement recalls are prevalent. Recalls have already been filed in 2024. Most generally, recalls are issued by the manufacturer and not by the FDA. Each can vary from one device to thousands of devices. 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, …

WebBetween 2002 and 2013, DePuy Synthes recalled 277 knee implant devices and components. Four of the recalls were labeled Class I, which indicates there is a reasonable probability that using the product may cause severe adverse health consequences or death. 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 …

Web16 jul. 2024 · The effectiveness of Persona in comparison to NexGen is currently being studied. 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. In other words, the plate was not staying in place. WebThe 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)

Web13 apr. 2024 · The ATTUNE™ Knee System is a modern knee system scientifically designed for STABILITY IN MOTION™ that more closely matches the kinematics of the natural knee to allow for functional knee restoration and improve patient satisfaction. Learn more about the ATTUNE™ Knee System STABILITY IN MOTION™

WebExactech has issued massive recalls for some of its knee, ankle, and hip replacement devices. Exactech Knee and Ankle UHMWPE Inserts. On February 7, 2024, Exactech sent an Urgent Medical Device Correction notice to knee and ankle surgeons, hospitals, and healthcare professionals. The notice informs readers that the company has expanded its … fisherlittleopeleeddieWebPatients who have undergone total hip replacement and are unsure if they received a Rejuvenate or ABG II modular-neck stem should contact their surgeon to confirm the product implanted. Stryker’s toll-free Patient Care Line can be reached by calling 1-888-317-0200 (U.S. and Canada only). The Patient Care Line is available from 8am–9pm … fisher line conditionerWeb26 apr. 2024 · In August 2024, medical device manufacturer Exactech ® recalled thousands of its knee and ankle replacement devices. The U.S. Food and Drug Administration (FDA) found that the devices, made with polyethylene inserts, may have been packaged in a way that exposed the inserts to too much oxygen. canadian rootsWebThe recall affected 3475 units of the knee replacement device. Patient complaints registered as adverse events with the FDA prompted the agency to investigate the … canadian royalties incWeb5 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); … fisher little bear wood stoveWebKnee Replacement Surgery. More than 5 million knee replacement surgeries were performed from 2000 through 2010. (1) The number of knee implants is projected to increase to 7.4 million by 2030. (2) Many of these procedures may result in complications requiring additional, revision surgery. Speak to an Attorney Now. fisher little joe regulatorWebRecalled Knee and Ankle Replacements. Exactech recalled all Optetrak, Truliant and Vantage brand knee and ankle replacement liners manufactured from 2004 to present. … canadian roshel senator