Many American's receive 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 could be a large number of reasons that your loved one, or even yourself, needed to receive a hip replacement made by Zimmer Durom. The procedure, which is known as either hip arthroplasty, or hip replacement more commonly, involves removing the original hip joint and replacing it with an artificially manufactured one. This process is done for a number of reasons, including arthritis pain, located in the joint, the normal wear and tear on the joint because of age, and as part of the treatment for a hip fracture.
The modern hip replacement operation has been taking place since the 1970's, which is why the idea may seem so commonplace to you. A hip replacement, such as those from Zimmer Durom, most commonly involves three separate pieces, designed to mimic how a natural knee joint would. They include a metal replacement for part of the femur. A component which allows for movement like the joint naturally would, and either bone cement or screws to hold the contraption in place.
One of the most common issues with hip replacements is the need for revision, or a further surgery to correct issues with the implant. Unfortunately, this is something many elderly and even healthy young patients cannot tolerate. It is the focus 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.
Though Zimmer Durom has maintained that this high failure rate is caused by surgeon error, it pulled the replacement from the market in July 2008 after its own internal study found that 8 percent of the devices needed revision in two years. This has let many doctors and lawyers to believe the issue is with the replacement.
If you or a loved one received a Zimmer Durom hip replacement, something your doctor will know, you may have the right to join a class action law suit, even if your replacement has not yet failed.. Be wary of signing anything by Zimmer Durom, as that may be a release taking away this right.
There could be a large number of reasons that your loved one, or even yourself, needed to receive a hip replacement made by Zimmer Durom. The procedure, which is known as either hip arthroplasty, or hip replacement more commonly, involves removing the original hip joint and replacing it with an artificially manufactured one. This process is done for a number of reasons, including arthritis pain, located in the joint, the normal wear and tear on the joint because of age, and as part of the treatment for a hip fracture.
The modern hip replacement operation has been taking place since the 1970's, which is why the idea may seem so commonplace to you. A hip replacement, such as those from Zimmer Durom, most commonly involves three separate pieces, designed to mimic how a natural knee joint would. They include a metal replacement for part of the femur. A component which allows for movement like the joint naturally would, and either bone cement or screws to hold the contraption in place.
One of the most common issues with hip replacements is the need for revision, or a further surgery to correct issues with the implant. Unfortunately, this is something many elderly and even healthy young patients cannot tolerate. It is the focus 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.
Though Zimmer Durom has maintained that this high failure rate is caused by surgeon error, it pulled the replacement from the market in July 2008 after its own internal study found that 8 percent of the devices needed revision in two years. This has let many doctors and lawyers to believe the issue is with the replacement.
If you or a loved one received a Zimmer Durom hip replacement, something your doctor will know, you may have the right to join a class action law suit, even if your replacement has not yet failed.. Be wary of signing anything by Zimmer Durom, as that may be a release taking away this right.
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