Coming Status Meeting In Stryker Lawsuit Litigation Lawyers at Schachter, Hendy & Johnson, P.S.C. are representing individuals who have been hurt by faulty cutting guides employed with Stryker Triathlon knee replacements. In April 2013, the Food and Drug Administration issued a Type I remember for the Stryker Triathlon knee replacement, which was used between 2010 and 2013. Class I recalls are the most serious recalls that are issued by the Food and Drug Administration. Patients who've obtained the Stryker Rejuvenate hip replacement device happen to be linked increased health risk because of the device's modular hip neck design failures which include fretting and corrosion. Plaintiffs of the Stryker Rejuvenate hip replacement apparatus allege that the apparatus has caused pain and/or puffiness as well as other consequences including metallosis, gangrene and osteolysis. Stryker is counseling patients who obtained the Rejuvenate and ABG II hip comes to get blood tests for elevated metal ion degrees and cross-sectional imaging to ensure the products are working properly, even if the patient isn't showing symptoms. Latest Upgrades The Stryker Accolade is experiencing failures that are extremely similar to those of the Stryker Rejuvenate and Stryker ABG II Modular Neck Hip Implants. The difference in breakdown appears to be where the hip implant breakdowns are happening. Predicated on information we've seen and from information supplied to us by hip implant litigation customers it appears that the Stryker Rejuvenate hip implant failures seem to largely occur at the intersection of the neck and come, whereas the Stryker Accolade hip implant breakdowns seem to largely happen where hip implants ball satisfies the stalk. Hip Implant Metallosis - Toxic Hip Implant Metal Poisoning If you are interested visit our site http://www.strykerlawsuit.org/ Stryker Rejuvenate hips have been reported to fail quickly, sometimes in a matter of a couple of years. Hip implants in general are expected to survive a couple of decades. Also, the Stryker Rejuvenate synthetic hip has been implicated by faulty product attorneys in a increased danger of metallosis, or metal intoxication. The Rejuvenate and ABG II hip implants are made differently than another metal on metal artificial hips as a result of their ceramic part that was used instead of just metal on metal layouts. In particular, they have a steel neck section that some merchandise defect attorneys have alleged can rub against the steel stalk shaving off small bits of steel and creating Metallosis. Stryker pronounced that it was recalling two products within the firm's Trident line. The Stryker Hip Implant component recall involves two hip-replacement cups - the Trident Acetabular PSL Cup and the Trident Hemispherical Cups - made at the Stryker facility in Cork, Eire. Neither of these recalls is immediately linked to the problems detected at the New Jersey plant, that could result in even more investigation into this difficulty. The Next Step if injured from a Stryker Rejuvenate and ABG II Hip Implant Our Facebook Page