Additional instructions included to inform all individuals of the recall within the organization, complete and return the enclosed Recall Notification Business Reply Form, and arrange for to return all affected devices to Stryker in Mahwah, NJ. One of them was when FDA issued a Class I recall for the Stryker ShapeMatch Cutting Guide device in 2013. Stryker Orthopaedics Modular Handle Triathlon Instruments, Non-Sterile, REF 6541-4-808, Lot 123, NDC M546654148080S Product Usage: Is a reusable instrument that is part of the Triathlon Primary total knee arthroplasty (TKA) system as well as the Triathlon Partial Knee Replacement (PKR) system. Knee replacement recalls have been issued because of loosening, early wear or faulty packaging. Friday, April 27, 2018 - The knee is the largest joint in the body and is expected to carry the full weight of an individual with every step. The company has paid billions of dollars to end metal-on-metal hip implant lawsuits. I tried unsuccessfully to contact Stryker, no contact info available anywhere, was on hold on customer service Why are some Knee replacement implants recalled? This was a disposable cutting guide designed to be used just once by a surgeon to guide and mark a bone before cutting it to fit the replacement knee. FDA Recalls of DePuy Knee Replacement System Depuy has been hit with several recalls of its knee replacement system. Knee Replacement Recall Process and Causes. Stryker Hip Replacement Recall. Faulty implant design. Posted on March 3, 2017 by CSSFIRM.COM. Failing to perform properly, faulty artificial knees put the health and safety of millions of individuals at risk. Stryker Orthopedics recalled the ShapeMatch Cutting Guide due to the risk of inaccurate bone cuts. 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. Mit einer Vielfalt von über 60.000 verschiedenen Produkten und Dienstleistungen zur medizinischen Versorgung von Patienten ist Stryker ein Pionier in der Medizintechnik. Last summer had knee replacement with Stryker Triathlon System which is loose, ill fitting, knocks when bend the knee, painful. Stryker ® Orthopaedics has voluntarily recalled its Rejuvenate modular and ABG-II modular-neck hip stem implants, according to the Food and Drug Administration (FDA). Patients may receive a poorly-fitting Triathlon Knee Replacement or suffer joint instability, looseness, fracture, pain, disability, or require revision surgery. A manufacturer may voluntarily recall a product when evidence is showing that it may be harmful to patients. Durch unsere innovativen Ideen erweitern wir die Möglichkeiten der modernen Medizin. The implant is designed to replace the function of a healthy knee. Flawed implant tool. It makes hip replacement implants and surgical instruments, among other products. A knee replacement recall can help establish legal liability against a … Since its launch in 2004, more than 2 million patients have received a Triathlon knee. Stryker Corp. is a large company based in Kalamazoo, Michigan with several divisions all in the area of medical technology. In January 2013, a Class I Stryker knee recall was issued, indicating that complications from the ShapeMatch system are so severe that they could cause serious health problems or death. Stryker Knee Replacement Recalls. Stryker indicates that fretting and corrosion (wear and tear) can occur within the devices, which can cause adverse tissue reactions and pain and swelling in certain individuals. Pain never goes away; throbbing, stabbing, shooting. Knee Replacement Recalls. Labeling errors (for instance, wrong size). Problems from the start. Cutting guides are used by knee replacement surgeons to position device components and mark the bone. Stryker® Hip Replacement Recalls And Lawsuits Stryker Corporation is a Michigan-based medical technologies firm known for its extensive line of total hip and knee replacement systems. Stryker Knee Replacement Recalls. Cutting guides are used by knee replacement surgeons to position device components and … Stryker designed these hip implants to … During total knee replacement (which is also called total knee arthroplasty), your surgeon removes the damaged surfaces of the knee joint and replaces them with metal and plastic components referred to as the prosthesis or implant.