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. Patients trust that a procedure such as this is so common and routine, they don't question their doctors opinions nor do they question the manufacturers of their joint replacements about the quality of the product being implanted into them. This has caused occurances that can injure you or someone else. 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. Be it arthiritis-related physical agony, or the 'wear and tear' of the joints on account of advanced years, or hip fractures - a common malady among the aged - this surgery is a solution for all of the above.
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. Included is a metal replacement of the femur. A bone cement or screws to hold the contraption in place allows movement like the joint naturally would.
Hip replacements commonly are in need for revision or further surgerys to correct issues. Regrettably, this is an issue that a lot of older people and actually healthy younger patients can't handle. This is the special target of the Zimmer Durom recall. 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. However, almost 12 percent of these patients needed surgery again within two years, prompting an outcry.
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. A study funded by the company found that 8 percent of patients needed a revision within two years. The theory is that the ensuing problems are more related to the replacement device rather than the surgeons who implant them.
If you or someone you know has had a hip replacement surgery in the last several years, ask your doctor if it was a Zimmer Durom. If it was, even if you have not had a failure of your hip replacement yet, you may be able to join a class action law suit. You will lose your rights if you sign a legal release by 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. Be it arthiritis-related physical agony, or the 'wear and tear' of the joints on account of advanced years, or hip fractures - a common malady among the aged - this surgery is a solution for all of the above.
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. Included is a metal replacement of the femur. A bone cement or screws to hold the contraption in place allows movement like the joint naturally would.
Hip replacements commonly are in need for revision or further surgerys to correct issues. Regrettably, this is an issue that a lot of older people and actually healthy younger patients can't handle. This is the special target of the Zimmer Durom recall. 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. However, almost 12 percent of these patients needed surgery again within two years, prompting an outcry.
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. A study funded by the company found that 8 percent of patients needed a revision within two years. The theory is that the ensuing problems are more related to the replacement device rather than the surgeons who implant them.
If you or someone you know has had a hip replacement surgery in the last several years, ask your doctor if it was a Zimmer Durom. If it was, even if you have not had a failure of your hip replacement yet, you may be able to join a class action law suit. You will lose your rights if you sign a legal release by Zimmer Durom.
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Get the scoop about pending class action lawsuits at this website about: durom lawsuits. Or check out zimmer durom hip replacement lawsuits info.
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