WebHip Replacement Recalls In 2010, Johnson & Johnson and its medical device subsidiary, DePuy Orthopaedics, recalled two acetyabular cups hip replacement systems because of their high rate of failures and new data showing a higher number of patients needing a second hip replacement. WebZimmer Holdings- Durom Acetabular Component (Durom Cup) Smith & Nephew- R3 Acetabular System; Biomet- M2a; Wright Medical- Conserve Plus Total Resurfacing Hip System; Wright Medical- Profemur Z Hip Stem; You may be entitled to compensation for these recalled or defective hip implants. Call today (216) 696-9330 or complete our hip …
Zimmer Durom Hip Implant Class Action - Klein Lawyers
WebNotice of Settlement to Class Members (French) If you received a Zimmer Durom hip implant, and have undergone further surgery to replace it (or are unable to undergo this replacement surgery for medical reasons), please telephone us at 604-874-7171 or toll free at 1-800-468-4466 or email us at [email protected]. WebSep 1, 2011 · High revision rates have also been reported with the Zimmer Durom, 11 the DePuy Pinnacle, 12 and for the smaller diameter (⩽ 46 mm) Smith & Nephew Birmingham Hip Resurfacing (BHR). 13,14 This ... small faces 1966 album
Out of joint: The story of the ASR The BMJ
WebJul 25, 2024 · Introduction: The aim of this study was to evaluate the incidence of adverse reactions to metal debris (ARMD) in a consecutive series of DUROM™ Hip Resurfacing Arthroplasty (HRA) at mid-term follow-up. Methods: Between October 2003 and March 2007 a total of 134 consecutive DUROM™ HRA in 121 patients were performed at our institution. WebMay 1, 2013 · Introduction. Hip resurfacing with a metal-on-polyethylene bearing, used in the 1970s, only had a 75% survival rate after five years [1].This was secondary to polyethylene wear and lead to this implant being abandoned in the 1980s [1].The performance of second-generation, metal-on-metal bearings in traditional hip implants in … WebRecall of DUROM HIP RESURFACING SYSTEM - ACETABULAR COMPONENT According to Health Canada (via FOI), this recall involved a device in Canada that was … small faces 1967