DePuy Hip Recall

The DePuy Hip Recall affects patients who have been implanted with either the DePuy ASR XL Acetabular system or the DePuy ASR Hip Resurfacing System. This hip recall has caused great concern among the patients who have been implanted with these devices.

The DePuy Orthopedics hip recall is due to the high revision rate of these two products. The revision rates reported by DePuy in the recall announcement indicate a 12% revision rate for patients who have been implanted with the DePuy ASR resurfacing system and a revision surgery rate of 13% for the patients who had received the DePuy ASR XL Acetabular system. (A revision surgery means that the hip replacement device has been removed and replaced by another hip implant device.)

However, the British Orthopedic Association has stated that the recalled ASR XL device has a revision rate of 21% after four years and 49% revision rate after six years.

Therefore, any patients who have had a hip replacement surgery since 2003 may be subject to the DePuy recall. There are approximately 93,000 individuals worldwide who have been implanted with these devices.

If you have been implanted with a recalled DePuy hip replacement system, or if you have a loved one who may have the defective device, the first thing to do is to contact your surgeon or your physician and verify that you have received a DePuy hip replacement device.

If you are certain that you have been implanted with one, the next step is to seek legal advice from an experienced hip recall lawyer who can help you by completing the form on the right. They will provide you with all the necessary information about your legal rights and help you get the compensation you deserve from the manufacturer of the defective hip replacement system.

Many patients have already filed claims for the compensation they deserve from the manufacturer of the defective hip replacement systems. Patients should contact a lawyer experienced in these cases prior to any revision surgery so the necessary actions can be taken to preserve the evidence that is needed to prove the case in court.  Delaying could dramatically hurt you and what you are entitled to.

If you are subject to the DePuy recall, it is advised that you act as soon as possible because state laws only allow a limited period of time for a patient to file a legal claim; once time expires no legal actions against the manufacturer of the defective hip replacement will be allowed.

Hip replacement patients may not recognize that there is a problem with their device because pain is not always associated with a failed hip replacement. If the patients do not contact a lawyer to represent them individually then the patients may end up being included in a DePuy ASR hip recall class action.  We will handle each case individually.

DePuy announced the recall of these hip replacements in August of 2010, approximately eight months after recalling the devices in Australia. The DePuy ASR XL hip replacement system and the DePuy ASR resurfacing system were both recalled. Many individuals have asked how the DePuy hip replacement might affect them, and the short answer is that they may require a hip revision surgery or have problems as a result of chromium and cobalt poisoning.

While DePuy may blame the high failure rate on surgical error, many believe that the failures are in large part due to the device’s poor design. It seems that surgeons from across the world are reporting high revision rates for the recalled DePuy hips. In fact, some noted medical engineers are now calling the DePuy ASR hip recall the largest disaster in the history of orthopedic devices. The patients are the victims of DePuy’s failure to properly test this device prior to releasing it for public use. Patients should contact an experienced hip replacement lawyer by filling out the form on the right to get a free consultation.

Hip recall lawyers can assist patients in becoming educated about this device and its effect on patients. Contact a hip recall lawyer by calling the 800 number listed above or by filling out the form on the right to get a free, no obligation consultation about the DePuy ASR hip recall. These lawyers know the steps that you need to take to protect your rights and can help you through the claim process and see to it that you get what you are entitled to.

Hip replacement has been a gift to people with joint problems for many years, and has increased the enjoyment that these people have received from life. Unfortunately, the very same procedure which has helped so many people can also cause much pain and suffering when a patient receives a faulty implant. After reading this post, you’ll know more about the DePuy ASR hip recall has announced the recall of two of their hip replacement systems, the ASR XL hip resurfacing system and the ASR acetabular component. While DePuy has said that the high failure rate is due in large part to surgeon error, significant evidence has come to light which leads many in the health community to believe that the implants themselves are to blame. If you are a victim of the DePuy ASR hip prosthesis, DePuy hip recall lawyers can help you with your situation.

Hip recall lawyers know about this product and its impact on their clients: they have been studying this implant since long before it was recalled, and continue to stay abreast of new developments both medically and legally. They can help clients with the process of pursuing and filing their claim against DePuy, and can walk them through many of the medical dangers of these hips. These lawyers will be there through the revision surgery and beyond, to see to it that each client receives the compensation they deserve for the trials their implant has caused.

Contact DePuy hip recall lawyers now to ensure that your rights are protected and to make sure you are compensated fairly for your pain and loss.

The DePuy hip recall of the ASR hip implant was announced by DePuy Orthopedics Inc. on August 26, 2010. The hip recall by DePuy of its ASR hip implant comes after the device was marketed for approximately six years between 2003 and 2010. The defective ASR hip system has been implanted in a total of about 93,000 patients, and the recall affects two products by DePuy: namely, the ASR Hip Resurfacing System and the ASR XL Acetabular System. This DePuy hip recall comes after years of published reports, studies and data indicating that the device was defective and failing in patients.

This DePuy hip recall was caused by the alarming number of complaints and high revision surgery rate for the device. DePuy statistics show that “approximately 12% of patients who had received the ASR resurfacing device and 13% of patients who had received the ASR total hip replacement needed to have a revision surgery.” This means that affected patients will undergo a painful and unnecessary DePuy hip revision surgery. Patients would not be facing this problem if not for the defective DePuy hip.

The ASR hip system has been manufactured and implanted in the United States since July 2003. This means that individuals who had their hips replaced on and after July 2003 should determine if they received a DePuy ASR and are affected by the DePuy ASR hip recall. You can contact your orthopedic surgeon or the hospital where the surgery took place to find out whether you received an ASR DePuy Hip. The next step is to hire your very own DePuy hip recall lawyer to help you protect your rights, and recover the compensation you deserve in a hip recall lawsuit against DePuy, the manufacturer of the device.