What products are part of the DePuy hip recall?
In August, 2010 DePuy Orthapaedics recalled two of its hip replacement devices: the ASR XL Acetabular System, and the DePuy Resurfacing System. The DePuy recall was based on the manufacturer receiving information that showed more people than expected were experiencing failure of the hip replacement devices.
What is the ASR XL Acetabular System?
This device is a ball and socket that consists of a femoral stem, the femoral head (ball) and the acetabular cup (socket).
What is the ASR Resurfacing System?
The ASR Resurfacing System consists of a cup that is placed over the natural femoral head (ball) and the acetabulum is replaced with a single piece cup.
What are some of the symptoms that could be experienced if the hip replacement device has failed?
- Adverse reaction to metal debris caused by accelerated wearing of the metal on metal design (including tissue and bone damage);
- Fracturing of surrounding bone;
- Dislocation of the device (the two components of the device are no longer properly aligned);
- Loosening of the implant (either does not remain in the correct position or does not stay attached to the bone).
How do I know if I have a potentially faulty DePuy hip replacement implant?
The ASR LX Acetabular System was first used in July 2003. If your surgery occurred after this date you should contact your surgeon to ascertain if a DePuy device was used for your surgery and you are affected by the DePuy recall. Your physician will want to follow up with you to determine if your hip replacement is functioning properly.
How will my doctor determine if the hip device is failing?
If you are experiencing symptoms yet are well past the initial healing period, it is important to determine the source of your symptoms. The doctor will perform an ex-ray to visually examine your hip. A blood test may also be ordered to test the metal ion levels of your blood (levels should be 7 parts per billion). The doctor will also be looking for evidence of soft tissue damage, and any abnormal masses that have formed within the hip.
What will happen if the doctor determines my hip device has failed?
Unfortunately, if the device has failed, it will be necessary to have a second revision surgery. The mechanism will need to be removed, along with any damaged tissue or bone. The postoperative care for your second surgery will be similar as for your first. Patients will undergo physical and occupational therapy and other forms of rehabilitation. Complications are possible, similar to your first surgery. However the success rate from a second hip surgery is lower than for the first because the bone may be weaker.
Do I need a lawyer?
While DePuy has stated that they will cover costs associated with monitoring and treatment, the damages you may experience may far exceed with what they are willing to cover. You will need to pursue any claims you may have for lost wages, pain and suffering or continuing disability. Contact the DePuy ASR Lawsuit Center to speak with a lawyer about what your options are. We are available to speak with you at your convenience, and your first consultation is completely free. If you decide to file a claim we will take your case on contingency, so you will pay nothing unless we win your case.
