Many citizens of the US get joint replacements each year. It is a way for elderly people, and for those who have overused their joints, to get more years of activity and enjoyment out of their lives. Because this procedure has become so routine, many do not question their doctors, or the manufacturers of their joint replacements about the quality of the technology that they are using. This has led to practices that can actually cause injury to you or your loved ones. If you know someone who has received a hip replacement, read on for this important information about the manufacturer Zimmer Durom.
There are many reasons that you or a loved one may have received a Zimmer Durom hip replacement, leading to danger for yourself of your loved ones. Hip replacement, also known as hip arthroplasty, is a common procedure in which the hip joint is removed and replaced by a prosthetic implant. This can be done for a variety of reasons, which include the pain of arthritis which was affecting the joint, damage to the joint over a long life, or the treatment of a hip fracture, an injury common to the elderly.
The current hip replacement surgery has been happening since the 1970's, which is why it may seem so ordinary to one. A Zimmer Durom hip replacement comprises three-part correction, is known to result in a behaviour similar to that of an original knee joint. The use a substitute part made of metal to replace a section of the femur bone. The device is held in place with screws and mimics the natual joint movement for the most part.
Hip replacements commonly are in need for revision or further surgerys to correct issues. Many older and even some young and healthy patients just can't tolerate it, unfortuately. This is primary with the recall of Zimmer Durom. The Zimmer Durom device was used by doctors in younger patients that would normally need a hip replacement, as it was designed to be long lasting. But more than 10% of these paitents are in need for having repeat surgery in the next 2 years.
In July of 2008, they ceased sales of the hip replacement device, although Zimmer Durom claimed that the high rate of failure is caused by surgeons' errors. Research paid for by the firm showed that a whopping 8% of those operated on required a correction in a couple years time. This has led many in the medical and legal communities to believe that the issue is with the replacement device and not with the surgeons.
In the event that you or an acquaintance had an operation to replace a hip in the past few years, inquire of your physician whether it was a Zimmer Duron. In the event that it was, whether your hip replacement has failed or not at this point, you can participate in a legal class action. If you are contacted by Zimmer Durom, do not sign their legal release, or you may lose this right. - 15438
There are many reasons that you or a loved one may have received a Zimmer Durom hip replacement, leading to danger for yourself of your loved ones. Hip replacement, also known as hip arthroplasty, is a common procedure in which the hip joint is removed and replaced by a prosthetic implant. This can be done for a variety of reasons, which include the pain of arthritis which was affecting the joint, damage to the joint over a long life, or the treatment of a hip fracture, an injury common to the elderly.
The current hip replacement surgery has been happening since the 1970's, which is why it may seem so ordinary to one. A Zimmer Durom hip replacement comprises three-part correction, is known to result in a behaviour similar to that of an original knee joint. The use a substitute part made of metal to replace a section of the femur bone. The device is held in place with screws and mimics the natual joint movement for the most part.
Hip replacements commonly are in need for revision or further surgerys to correct issues. Many older and even some young and healthy patients just can't tolerate it, unfortuately. This is primary with the recall of Zimmer Durom. The Zimmer Durom device was used by doctors in younger patients that would normally need a hip replacement, as it was designed to be long lasting. But more than 10% of these paitents are in need for having repeat surgery in the next 2 years.
In July of 2008, they ceased sales of the hip replacement device, although Zimmer Durom claimed that the high rate of failure is caused by surgeons' errors. Research paid for by the firm showed that a whopping 8% of those operated on required a correction in a couple years time. This has led many in the medical and legal communities to believe that the issue is with the replacement device and not with the surgeons.
In the event that you or an acquaintance had an operation to replace a hip in the past few years, inquire of your physician whether it was a Zimmer Duron. In the event that it was, whether your hip replacement has failed or not at this point, you can participate in a legal class action. If you are contacted by Zimmer Durom, do not sign their legal release, or you may lose this right. - 15438
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