List of recalled knee replacements

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August undefined, 2024

WebDefective Stryker Knee Replacements. Recipients of defective Stryker knee replacements who experience any symptom of device failure such as serious throbbing pain, difficulty standing or moving, or feeling of instability should contact their implanting surgeon and a knee implant recall lawyer for immediate consultation. WebThe personal injury attorneys at Rosenfeld Injury Lawyers, LLC, are advocates for injured patients harmed by defective medical devices. Contact defective medical device lawyers at (888) 424-5757 to schedule a free consultation and discuss your legal options for initiating a hip implant case. We specialize in Stryker lawsuits.

What is the Exactech Knee Device that has been Recalled?

WebLearn how to know if your knee replacement has been recalled and why you may need a lawyer if you’ve been injured by a defective knee replacement device. Toll-Free: 888-904-6847. Phone: 508-283-5500. … WebPatients 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 … htcu westyorkshire.pnn.police.uk

Exactech Recalls 140,000 Knee Replacements for Failure Risk

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. 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... 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) htc u ultra s-on

Smith & Nephew’s Knee Replacement Device Recalled

Johnson & Johnson

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... Web5 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); … hockey life cambridgeWeb28 mrt. 2024 · Which Exactech Knee Replacement are Recalled? The recalled Exactech Knee replacements include: OPTETRAK Comprehensive Knee System; TRULIANT … hockey life crossiron mills

"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. " - List of recalled knee replacements

List of recalled knee replacements

Knee Replacement Surgery & Knee Pain Treatment in Ohio

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 …

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Web13 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 ... Web26 jun. 2024 · Knee replacement surgery remains one of the most commonly performed replacement surgeries in the U.S., following its introduction in the 1970s. Smith Nephew Oxinium devices were offered from January 2000 until recall in September 2003, and the affected cementless devices should no longer be used.

Web23 feb. 2024 · Potential problems caused by Exactech’s recalled knee and ankle implants include: Accelerated wear, debris production, bone loss, component fatigue and … WebRecalled Knee and Ankle Replacements. Exactech recalled all Optetrak, Truliant and Vantage brand knee and ankle replacement liners manufactured from 2004 to present. …

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. 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 …

Web31 okt. 2024 · Smith & Nephew’s first-generation knee replacement device was recalled on Oct. 1 as the Food and Drug Administration announced the Class 2 device recall online, following a series of research and tests regarding the high failure rate of the device.. Smith & Nephew’s JOURNEY Bi-Cruciate Stabilized (BCS) Knee system was the first-generation …

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. htc v36bml 128 ship s-onWeb23 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, … htc vitality hubWeb10 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. hockey life edmonton westWebOn February 7, 2024, Exactech expanded a voluntary recall on all Optetrak, Logic, and Truliant knee replacements and Vantage total ankle replacements packaged in defective bags regardless of a ... htc verizon phoneWebKnee surgery patients who had an Exactech knee implant that failed and need revision surgery may be entitled to bring a lawsuit and seek financial compensati... htc v20 accessoriesWebLargest Knee Recalls Since 2015 January 2016 Device: Zimmer NexGen Complete Knee Solution Cruciate Retaining (Cr)Flex Femoral Components Number Recall: 42,064 … htc verizon wireless xv6800 driverWebYou 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 ... hockey life edmonton south