Mesothelioma Legal Advice

Stockholders, doctors, patients, and attorneys are still debating the handling of the sale of Zimmer Durom Cup hip implants in the United States. Although these devices were used successfully in Europe for three years prior to being approved in the U.S., their track record in America has been less than stellar. Many contend that the company was slow to respond to the problems that were occurring and negligent in informing the public about what was going on. Many feel that a recall should have been issued on the defective cups, but Zimmer has not done so.

Even though Zimmer knew about the problem as early as January, 2008, it wasn’t until July of that same year that they finally suspended American sales of the device. They chose to spend the interim time looking into the allegations instead of eliminating the problem. They were skeptical that the implants could be defective as doctors were saying, because they had been used so successfully in Europe. Since they felt they needed to look elsewhere for the problem, they didn’t want to take the devices off the market until they were sure what the culprit was.

Using information taken from 3,100 implant surgeries, Zimmer put together a database of material so that their researchers could study the problem in detail. After a great deal of study, they determined that there was nothing wrong with the implant technology. What they found was that American doctors hadn’t received adequate training prior to starting to perform the surgeries. The implants had been designed differently from previous types of hip replacement devices, and surgeons needed to be much more precise about the way they implanted them than they’d ever needed to be before.

Since there was no evidence found saying that the implant device itself was to blame for the problems patients were having, no recall was ever issued. This leaves the way clear for them to put the implant back on the market once efficient methods of training are developed for doctors. Zimmer needed to develop a better way of teaching physicians the very precise skills required to do the hip replacement using the Durom Cup successfully.

Part of the problem resulting in the public demand for recall is that no follow-up procedures were put in place by Zimmer in order to track the progress of patients using their implants. Some may argue that it isn’t their job to police the product after it has been implanted, but others feel that if they made it, they should continue to be responsible for its performance.

Physicians clearly blame the device for the problems that are popping up. They point to the fact that a knee replacement device manufactured by Zimmer is still being used in the United States even though Austrian doctors stopped using it just three years after it was introduced because it failed in almost 40% of the cases in which it had been used. It’s easy to understand why doctors are feeling uneasy about using Zimmer products despite their previous reputation.

Zimmer holdings has released a recall of their Zimmer Durom cup hip implant.  There are Zimmer hip lawsuits pending in multiple states across the US.  If you or a loved on has been subject to a Zimmer Durom implant, then you may want to contact a Zimmer Hip Lawyer to see if you have a case.

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In 2006 Zimmer Holdings, the world’s largest manufacturer of orthopedic devices, introduced the Zimmer Durom Cup Hip Implant in the United States. Since that time, thousands of implants have been surgically inserted into American patients. The device had been used successfully in Europe since 2003 before being tried in the U.S. Unfortunately, its road to success has been far bumpier in the U.S. than it has been in Europe, and U.S. sales have been put on hold.

Physicians who performed the unsuccessful surgeries claim that the Zimmer Cup is a defective piece of equipment. Zimmer counters with the fact that it has been so successful in Europe and contends that the surgeons must be at fault. They do agree, however, that surgeons have not had access to adequate training in the correct procedures to use when performing the implant and that this lack of training has been instrumental in the failure of the replacement surgeries. With this fact in mind, Zimmer voluntarily suspended U.S. implant sales until a method of training surgeons is in place. Sadly, some surgeons are still blaming the device itself and are unwilling to perform more implant surgeries no matter what kind of training they are offered.

Zimmer holdings has released a recall of their Zimmer Durom cup hip implant.  There are Zimmer hip lawsuits pending in multiple states across the US.  If you or a loved on has been subject to a Zimmer Durom implant, then you may want to contact a Zimmer Hip Lawyer to see if you have a case.

Under the laws of most states, patients who suffer from the effects of defective orthopedic devices are entitled to compensation if the device doesn’t perform as expected. These laws state that patients can be compensated for pain and suffering, medical bills, and lost wages if it is the device that is at fault. So, the battle goes on with Zimmer claiming there is nothing wrong with the design of the Durom Cup and with physicians blaming the device for the failed surgeries.

Hip replacement surgeries aren’t a new idea. In fact, as early as 1891 there is written reference to attempts to replace the femoral head using ivory devices. It wasn’t until 1960, however, that the Burmese surgeon, Dr. San Baw, started replacing broken hip bones with ivory. Within the next 20 years Dr. Baw claimed a success rate of 88% on the more than 300 replacement surgeries that he performed.

Modern hip replacement devices owe their origin to John Charnley who pioneered a 3-part artificial hip joint. Developed in the 1970s, this device or an adaptation of it was used all over the world for over 20 years. Then, in 2003, Zimmer introduced the Durom Cup which was touted as the best hip replacement device ever created during its initial try-outs in Europe.

There has been a vast improvement in both hip replacement devices and the surgical methods used to implant them in the years since the first procedures were performed, but the operation still has its problems. The most common problem patients with a Zimmer Durom Cup implant have is in the implant slipping. This occurs due to the fact that the implant is built smaller than the patient’s original bones, and if it isn’t inserted correctly, it can move around. In addition, the implant can sometimes loosen and infections can occur. In spite of the risks involved with this surgery, physicians still prefer that the patients who have serious problems with their hip joints undergo the procedure.

Zimmer can only hope to win the lawsuits that have been filed against it and be able to market their Durom Cup more successfully in the U.S. in the future. They still believe that their device can make a positive difference in the lives of many people if used correctly.

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