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Wright Hip Lawsuit News: Bernstein Liebhard LLP Notes Issuance of New Order in Federal Wright Conserve Hip Replacement Litigation
Date:5/21/2013

p>On January 17th, the U.S. Food & Drug Administration (FDA) cautioned that metal debris released by all-metal hips can damage the bone and/or soft tissue surrounding the implant and joint, leading to adverse local tissue reactions, premature device failure, and even additional symptoms or illnesses elsewhere in the body. Among other things, the FDA cautioned doctors to consider metal ion testing if patients are experiencing symptoms of hip implant failure.*

In addition to Wright Conserve hip lawsuits, Wright Medical Group dislosed in an April 30th regulatory filing that is also facing a growing number of claims involving the Wright Profemur hip replacement system.** On March 20th, a Joint Notice of Settlement filed with the U.S. District Court, Northern District of California, reporting that one lawsuit involving a Profemur hip product had been resolved ahead of trial. (Tucker, et ux. v. Wright Medical Technology, Inc., et al., No. 4:11-cv-03086) In the April 30th filing, the company warned that last year’s Stryker hip recall for Rejuvenate and ABG II hip stems could potentially affect sales of its Profemur modular-neck stems, as that recall has led to additional scrutiny of cobalt chrome modular neck products, such as the Profemur hips.**

Hip implant patients who experienced complications related to Wright Profemur hip replacements or Wright Conserve hips may be entitled to compensation for medical bills, lost wages, pain and suffering and other damages. For more information on filing a Wright hip lawsuit, please visit Bernstein Liebhard LLP’s website, or call one of the Firm’s attorneys today for a free case review, at 800-511-5092.

*fda.gov/MedicalDevices/ProductsandMedicalProcedures/ImplantsandProsthetics/MetalonMetalHipImplants/ucm241604.htm
**

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