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Wednesday, February 18, 2009

Zimmer Durom Recall - Get Compensated

By Maxwell Schmickman

Many American's receive joint replacements each year. It is a method for senior citizens or anyone with worn out joints to obtain additional years of being active and enjoying life. 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 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. A common procedure in which the hip joint is removed and replaced by a prosthetic implant is the hip replacement, also known as hip arthroplasty. 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 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. 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. Regrettably, this is an issue that a lot of older people and actually healthy younger patients can't handle. This is primary with the recall of Zimmer Durom. The Zimmer Durom implant was supposed to be durable and was understandably, advocated for younger recipients, whose conditions warranted such surgeries. But more than 10% of these paitents are in need for having repeat surgery in the next 2 years.

Though Zimmer Durom has stated that this high failure rate is a caused by surgon error, they stopped selling their hip replacement device in July 2008. 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.

In the last several years you or someone you know had a hip replacement, ask your doctor if it was done by 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. If you are contacted by Zimmer Durom, do not sign their legal release, or you may lose this right.

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