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.
In most U.S. states, laws are in place to help patients who suffer due to defective prosthetic devices. The laws are designed to compensate them for pain, medical expenses, and the loss of wages caused by their problems with orthopedic procedures resulting from a malfunction of a prosthetic device. Zimmer, while not admitting to producing an inferior product based on its success rate in Europe, voluntarily pulled the cup from the U.S. markets in July, 2008 pending further investigation.
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.
Physicians who have already performed exploratory surgeries to determine the cause of their patients' problems have discovered that many of the cups have loosened a great deal over time. In fact, one doctor reported that he found a cup that had loosened so much that it popped from its socket when he touched it. In other patients surgeons have found that the device has actually migrated a short distance within the body. Zimmer cites the success of the cup in Europe as basis for its belief that there is nothing defective about the device, but physicians believe that almost 6% of all Durom Cups will fail and need revision surgery within the next couple of 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.
In most U.S. states, laws are in place to help patients who suffer due to defective prosthetic devices. The laws are designed to compensate them for pain, medical expenses, and the loss of wages caused by their problems with orthopedic procedures resulting from a malfunction of a prosthetic device. Zimmer, while not admitting to producing an inferior product based on its success rate in Europe, voluntarily pulled the cup from the U.S. markets in July, 2008 pending further investigation.
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.
Physicians who have already performed exploratory surgeries to determine the cause of their patients' problems have discovered that many of the cups have loosened a great deal over time. In fact, one doctor reported that he found a cup that had loosened so much that it popped from its socket when he touched it. In other patients surgeons have found that the device has actually migrated a short distance within the body. Zimmer cites the success of the cup in Europe as basis for its belief that there is nothing defective about the device, but physicians believe that almost 6% of all Durom Cups will fail and need revision surgery within the next couple of 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.
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