It is important to know what type of hip surgery that is indicated for ones condition, what the procedure is going to be, what the device is going to be used and what are the good and bad consequences to be expected. The size of the hip cup used in a hip replacement procedure was found to be a factor for the likely occurrence of complications as expressed in the DePuy hip replacement update. There are different types of hip replacement operations with consequent size and type of hip cup that are employed by surgeons at present. A hip resurfacing operation is one of the many hip arthroplasty methods used.

The Process Of Hip Resurfacing

The good thing about this method is that there is less bone removed for the implant to be placed. For those who are not legible for a total hip arthroplasty, the most common hip replacement operation, a hip resurfacing surgery is an alternative option. The two actually have a lot of similarities. They differ, however, in the amount of bone to be removed in the operation. They differ also in the hip cup used wherein in the case of the hip resurfacing management, a cobalt-chrome metal composes the hip cup. The hip cup mimics a femoral head that us why it is hollow and mushroom-shaped. If revision of the hip device is needed, the surgeon can work with ease since there is enough bone parts of the femur left for them to work on.

Another noted advantage of this intervention is that the size of the hip cup used is large and very similar to an original one that is why dislocation is avoided. Total hip replacement uses articular interface with sizes 28 mm, 32 mm and 36 mm and dislocation is a common complication. But all in all, the greatest advantage of this operation is the bone conserving characteristic of hip resurfacing surgery.

DePuy Orthopaedics used to manufacture the hip devices ASR XL Acetebular Hip System and ASR Hip Resurfacing System but since the release of the DePuy hip replacement recall, these alleged defective and badly-made products were removed from the market. If you feel the need to file your case, you can actually contact a skilled and efficient hip replacement lawyer. For more information about the recall and lawsuits, visit related sites available.
 
Many people are already aware that DePuy Orthopaedics, a subsidiary of Johnson & Johnson, have globally recalled their ASR XL Acetabular System and the ASR Hip Resurfacing System.A DePuy lawsuit is even filed by a recipient in Australia in response to it.The National Joint Registry for England and Wales revealed their high five-year failure rate.That would mean that 1 in 8 recipients require a revision surgery to correct the damage caused by the DePuy implants.

DePuy established a claims process immediately hoping that recipients would choose not to file lawsuits instead. But DePuy have only offered to reimburse “reasonable and customary” expenses that are related to your hip device. Each claim is subject to an eligibility review and the amount recipients would receive is solely up to the company.What's worse, evidence you sign over to DePuy might be used against you to devalue your claim.

Seeing a lawyer would help you in recovering compensatory damages DePuy has a legal obligation to give.These are some of the damages a lawsuit can help you get:

Medical costs: hospital bills, physical therapy, follow-up appointments with your doctor, hiring a caregiver, tests on your hip (including blood tests, x-rays, and an MRI), and revision surgery.

Travel costs: costs related to travel to and from your doctor, medical specialist, or any other place you travel to for tests and/or treatment related to the ASR recall.

Pain and suffering: mental anguish, physical pain, the inability to enjoy your life as you once did, loss of independence, and damaged relationships.

Loss of income: past, present, and future lost wages related to your ASR testing, treatment, and recovery.

Disfigurement and scarring: caused by your revision surgery.

If you had undergone a hip replacement surgery after July 2003, you could be a recipient of a DePuy hip implant. Your orthopedist and even the hopital where your hip replacement surgery was performed could provide you with this information.To learn more about the DePuy case you can visit the hip replacement recall center.

 
The US Senate examined the FDA approval process of the DePuy hip replacement system last April 13, 2011. The Food and Drug Administration’s (FDA) now infamous 510(k) premarket approval process, which DePuy Orthopaedics and other medical device manufacturers use to send their products to the market without subjecting them clinical trials was covered in a scheduled hearing made by the senate. Of course, a lot of us will agree that this hearing was quite predictive and many of us have been waiting for it because DePuy’s defectively designed hip replacement systems have affected thousands of people.

A special committee was created just for this case and this committee gathered people to testify against this particular medical device. Most of those who testify believe that for medical devices that underwent an approved through the 510(k) process were more likely to be subject to a recall than those that underwent clinical trials. After thorough investigations, the special committee concluded, “Internal reviews by FDA officials and other outside sources have found troubling lapses in the procedures by which a number of medical devices were approved,” and that, “the results of these investigations caused procedural and management changes to be implemented at the Center for Devices and Radiological Health in recent months.”

The move of the US government that takes the DePuy recall with the seriousness it deserves is taken positively by a lot of hip recall lawyers. However, these lawyers still believe that doesn’t do much for those who have already suffered injuries due to their hip replacements. So, for people who wants to be compensated for the damages created by this product, contact a hip replacement recall lawyer immediately.