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De puy asr hip recall revision surgery

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DePuy ASR Hip Recall Revision Surgery<br />http://depuyhiprecallsite.com/<br />DePuy Orthopaedics was founded 1895. It was the first commercial orthopaedics company in the U.S. that pioneering spirit. Their long-standing commitment to innovation…
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  • Added: May, 12th 2011
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  • Tags: depuy hip lawsuit, depuy hip recall, depuy hip, hip recall revision, depuy hip lawyers, depuy hip class action, hip recall, depuy asr hip recall, hip recall settlements, hip recall class action
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by: depuyhiprecallnews, 2 pages

http://www.depuyhiprecallcenter.com One of the MoM hip implant designs getting a bad press is the faulty articular surface replacement (ASR) hip made and marketed by DePuy Orthopaedics, a subsidiary ...

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  1. DePuy ASR Hip Recall Revision Surgery<br />http://depuyhiprecallsite.com/<br />DePuy Orthopaedics was founded 1895. It was the first commercial orthopaedics company in the U.S. that pioneering spirit. Their long-standing commitment to innovation in patient care has helped them become a global leader in orthopaedic devices and supplies, including hip, knee, extremity, trauma, cement, and operating room products.<br />Earlier this year, it has been reported that DePuy has started pulling out their defective products. The company had stopped selling the system in late 2009. On the 26th of August 2010, they officially announced the recall of their malfunctioning hip replacement systems.<br />The DePuy hip recall was of the ASR hip implant. It comes after the device was marketed for about six years between 2003 and 2009. The defective hip system has been implanted in a total of about 93, 000 patients.  This hip recall affects two products by DePuy namely, the ASR Hip Resurfacing System and the ASR XL Acetabular System. This DePuy hip recall comes after years of published reports, studies and data indicating that the device was defective and failing in patients. The reason for this DePuy hip recall is because of the alarming number of complaints and high revision surgery rate for the device. DePuy statistics show that “approximately 12% of patients who had received the ASR resurfacing device and 13% of patients who had received the ASR total hip replacement needed to have a revision surgery.” <br />After this cliff-hanger, DePuy Orthopedics issued for a hip recall revision. This means that affected patients will undergo a painful and unnecessary DePuy hip recall revision surgery.  Of course, this problem should have been fixed with the initial surgery if not for the defective DePuy hip. <br />In addition, DePuy recommends yearly monitoring " to ensure the ASR hip replacement is functioning well, even in the absence of symptoms." <br />However, DePuy stated in the release that few of these devices remain on the worldwide market due to its decision last year to discontinue the ASR system as a result of declining demand and other factors.<br />President of DePuy Orthopaedics Inc. also stated in the release that they are committed to assisting patients and health care providers by providing information through multiple channels and paying for the cost of doctor visits, tests and procedures associated with the hip recall revision.<br />

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