In 2006 Zimmer Durom Cup Hip Implants were approved for use in the United States. Within less than 2 years, more than 12,000 patients were functioning using a Durom Cup as a replacement device for a defective hip joint. Although these implants had been used for 3 years in Europe prior to being approved in the U.S. and had exhibited a high rate of success, in the U.S. patients started developing problems, some almost immediately after surgery. Their doctors, looking for reasons why the implants failed, decided that the Durom Cup was a defective device.

Patients who suffer from the use of defective prosthetic devices are protected by law in most U.S. states. These laws entitle a patient who experienced pain, incurred medical expenses, or lost wages due to a defect in a medical device to receive compensation for their losses. Zimmer has not yet conceded that their product is defective because of its success rate in the European market, but in order to give itself time to develop a better training program for American surgeons, Zimmer voluntarily pulled the cup from the American market in July, 2008.

If you perform a search on the Internet for “Zimmer Durom Cup Lawsuits”, you will find a host of attorneys who are looking to help file lawsuits against Zimmer on behalf of patients. As the number of cases of implant failures continues to grow, these attorneys have done their research and believe that they can file successful individual or class action lawsuits against the manufacturer.

Some physicians have performed exploratory surgeries to try and determine what is causing their patients so much trouble. In some cases they have discovered that the cup has become so loose in the socket that it just pops out when touched. In other cases, the entire device has been found to have migrated a short distance away from where it should be located. Since the device has reputedly been so successful in Europe, Zimmer continues to deny any wrongdoing. Even so, physicians have estimated that almost 6% of the Durom Cup implants will fail and need revision within the next few years.

People who own Zimmer stock have come to believe that the company was negligent in waiting until July, 2008 to pull the product off the American market. They and their attorneys feel it should have been pulled prior to January 22, 2008. Because of this belief, stockholders in Indiana have filed a class action lawsuit asking that damages be paid to those investors who bought stock between the January date and July, 2008 when the problem was announced and the product taken from the market.

Zimmer is still taking the position that its product is not defective. Instead they believe that the inadequate training given to physicians prior to performing the procedure is to blame. With this in mind, Zimmer announced in October, 2008 that it would be setting aside $47.5 million in order to pay off lawsuits resulting from the surgical failures referring to a July report which said that as much as 5.7% of the surgeries could require revision. This fund has been earmarked to pay for “revisions associated with surgeries that predate the company’s voluntary suspension and which also occur within two years of the original surgery date.

Zimmer Holdings, Inc., the world’s largest manufacturer of orthopedic devices, introduced its Durom Cup Hip Implant in 2003 in Europe. Three years later, in 2006, it was approved for use in the United States. From the onset, however, U.S. procedures were plagued with problems. Within the first two years of its use, 12,000 of the devices were implanted, and within a few months, many of them began to fail. In an attempt to explain the numerous surgical failures, doctors finally that the Durom Cup is a defective product.

Most states within the U.S. have laws designed to help patients who incur pain and suffering caused by defects in prosthetic devices. Per these laws, patients are entitled to compensation for their pain, medical expenses, and lost wages if it can be proven that a defective implant was to blame for their problems. Although Zimmer still stands fully behind its device based on its track record in Europe, it voluntarily pulled the product from the American market in July, 2008 in order to develop better training methods for doctors who insert the implants.

By using Google to search the Internet for “Zimmer Durom Cup Lawsuits” you can find many websites of attorneys who feel that patients have a case against Zimmer and offer to help them file lawsuits. The number of implant failures continues to grow, and these attorneys who have taken it upon themselves to become involved truly believe that Zimmer is at fault. Physicians tend to agree and estimate that hundreds of the devices will fail within the next few years.

Some physicians have performed exploratory surgeries to try and determine what is causing their patients so much trouble. In some cases they have discovered that the cup has become so loose in the socket that it just pops out when touched. In other cases, the entire device has been found to have migrated a short distance away from where it should be located. Since the device has reputedly been so successful in Europe, Zimmer continues to deny any wrongdoing. Even so, physicians have estimated that almost 6% of the Durom Cup implants will fail and need revision within the next few years.

Stockholders in Zimmer stocks feel that the company did not pull the product from the market quickly enough causing additional problems for patients. With this feeling in mind, stockholders filed a class action lawsuit in Indiana seeking damages for those who invested in company stocks between January and July, 2008. These stockholders and their attorneys believe that Zimmer should have suspended sales before January 22, 2008 when a large number of problems began to surface.

Zimmer is still taking the position that its product is not defective. Instead they believe that the inadequate training given to physicians prior to performing the procedure is to blame. With this in mind, Zimmer announced in October, 2008 that it would be setting aside $47.5 million in order to pay off lawsuits resulting from the surgical failures referring to a July report which said that as much as 5.7% of the surgeries could require revision. This fund has been earmarked to pay for “revisions associated with surgeries that predate the company’s voluntary suspension and which also occur within two years of the original surgery date.

In 2006 Zimmer Durom Cup Hip Implants were approved for use in the United States. Within less than 2 years, more than 12,000 patients were functioning using a Durom Cup as a replacement device for a defective hip joint. Although these implants had been used for 3 years in Europe prior to being approved in the U.S. and had exhibited a high rate of success, in the U.S. patients started developing problems, some almost immediately after surgery. Their doctors, looking for reasons why the implants failed, decided that the Durom Cup was a defective device.

Patients who suffer from the use of defective prosthetic devices are protected by law in most U.S. states. These laws entitle a patient who experienced pain, incurred medical expenses, or lost wages due to a defect in a medical device to receive compensation for their losses. Zimmer has not yet conceded that their product is defective because of its success rate in the European market, but in order to give itself time to develop a better training program for American surgeons, Zimmer voluntarily pulled the cup from the American market in July, 2008.

By using Google to search the Internet for “Zimmer Durom Cup Lawsuits” you can find many websites of attorneys who feel that patients have a case against Zimmer and offer to help them file lawsuits. The number of implant failures continues to grow, and these attorneys who have taken it upon themselves to become involved truly believe that Zimmer is at fault. Physicians tend to agree and estimate that hundreds of the devices will fail within the next few years.

Doctors who have done further surgery to determine the cause of patient discomfort have found that the cups have loosened over time to the point where they just pop from the sockets at the slightest touch. Other patients have devices which have actually migrated a short distance in their bodies so they are no longer located exactly where they should be. Although Zimmer contends that the rate of failure of the Durom Cup is quite low, physicians believe that hundreds of them will fail and need revision within the next few years.

Stockholders in Zimmer stocks feel that the company did not pull the product from the market quickly enough causing additional problems for patients. With this feeling in mind, stockholders filed a class action lawsuit in Indiana seeking damages for those who invested in company stocks between January and July, 2008. These stockholders and their attorneys believe that Zimmer should have suspended sales before January 22, 2008 when a large number of problems began to surface.

Zimmer still pleads its case that its Durom Cup is not to blame for the surgical failures in the United States. Instead they contend that physicians did not receive adequate training for doing the procedure. Even so, in October, 2008, Zimmer announced that it had reserved $47.5 million to pay claims won in lawsuits against it. In July it was shown that the failure rate of cup implants could be as high as 5.7%. Zimmer states that this money is not being reserved for all patients and revisions but only for “revisions associated with surgeries that predate the company’s voluntary suspension and which also occur within two years of the original surgery date.” The resolution of this problem remains to be seen.

Zimmer Durom Cup Hip Implants had been used successfully in Europe for 3 years prior to being approved for use in the United States in 2006. Less than two years later, the device had already been implanted in more than 12,000 American patients, and numerous problems with the implants were already beginning to surface. American doctors started searching for reasons the procedures had failed and pinpointed the cup as a defective product that was prone to problems.

Patients who suffer from the use of defective prosthetic devices are protected by law in most U.S. states. These laws entitle a patient who experienced pain, incurred medical expenses, or lost wages due to a defect in a medical device to receive compensation for their losses. Zimmer has not yet conceded that their product is defective because of its success rate in the European market, but in order to give itself time to develop a better training program for American surgeons, Zimmer voluntarily pulled the cup from the American market in July, 2008.

There are many websites on the Internet of attorneys who feel they can help patients file successful suits against Zimmer. Perform a search using the keywords “Zimmer Durom Cup Lawsuits” if you’d like to contact one of them. The number of failed implants is growing, and these attorneys who have researched the problem believe that patients have a good case against the company. Many physicians are in agreement with the attorneys as they estimate that within a few years’ time hundreds of the devices will fail causing revision surgery to become necessary.

Some physicians have performed exploratory surgeries to try and determine what is causing their patients so much trouble. In some cases they have discovered that the cup has become so loose in the socket that it just pops out when touched. In other cases, the entire device has been found to have migrated a short distance away from where it should be located. Since the device has reputedly been so successful in Europe, Zimmer continues to deny any wrongdoing. Even so, physicians have estimated that almost 6% of the Durom Cup implants will fail and need revision within the next few years.

Zimmer stockholders take the position that Zimmer should have announced a suspension of U.S. sales before January 22, 2008 instead of waiting until July. Because of this belief, they have filed a class action lawsuit in Indiana requesting damages for those investors who purchased stock between January 22 and July, 2008 when the product was finally pulled from the market.

Zimmer still pleads its case that its Durom Cup is not to blame for the surgical failures in the United States. Instead they contend that physicians did not receive adequate training for doing the procedure. Even so, in October, 2008, Zimmer announced that it had reserved $47.5 million to pay claims won in lawsuits against it. In July it was shown that the failure rate of cup implants could be as high as 5.7%. Zimmer states that this money is not being reserved for all patients and revisions but only for “revisions associated with surgeries that predate the company’s voluntary suspension and which also occur within two years of the original surgery date.” The resolution of this problem remains to be seen.