subject: Zimmer Hip Recall Warning [print this page] Zimmer Hip Recall Warning Zimmer Hip Recall Warning
Zimmer Holdings is a multinational company and one of the largest manufacturers of orthopedic devices in the U.S. More than 13,000 patients nationwide have had a Zimmer Hip implant. Research indicates that between 5 and 8 percent of these implants are defective in terms of the Durom Cup components. This Zimmer Hip Complication involves an improper bond between the patient's bone and the cup. This causes the Cup and hip bone to loosen and separate which in turn causes pain as these two loose components rub against each other. Make sure to keep up with breaking news on Zimmer hip problems and watch for a possible Zimmer Hip Recall.
Zimmer Hip Complications were brought to the attention of the public in April of 2008. Dr. Dorr, a respected orthopedic surgeon wrote a letter to the American Association of Hip and Knee Surgeons warning about the failure rates that he had seen with Durom Cups. By July 2008, Zimmer stopped selling its Durom Cup component and issued a press release saying they were temporarily suspending marketing and distributing the Cup in the U.S. on a voluntary basis. Zimmer goes on further to say they will be providing more detailed surgical techniques and instructions to surgeons for further training. It would appear that Zimmer is not willing to take responsibility for device failure but rather has shifted blame to the surgeons.
Zimmer has not issued a Zimmer Hip Recall for it Durom Cup component as of yet. Patients who have had a Zimmer Hip Implant and experienced a Zimmer Hip Complication could have problems with Cup loosening and may have to have additional surgery because of the company's negligence. Additional surgeries are estimated to cost between $30,000 and $40,000.
Zimmer has begun an aggressive legal maneuver and attempting to contact patients directly and obtain releases of liability. Make sure you consult with an attorney before signing your rights away. It is believed that Zimmer failed to warn physicians and consumers about the associated risks with the Durom Cup and should be held accountable for injuries they have caused. Lawsuits have been filed against Zimmer for damages patients have sustained as a result of a Zimmer Hip Complication. If you would like additional information about the Zimmer Durom Cup and possible Zimmer Hip Recall, you should consult with a Zimmer Hip attorney.
If you have experienced a Zimmer Hip Complication such as Durom Cup loosening, severe hip pain, or prosthetic fracture make sure you contact a Zimmer Hip attorney to see if you qualify for a Zimmer hip lawsuit. Given that Zimmer has suspended distributing and selling of the Durom Cup in the U.S., this may be an early sign of a Zimmer Hip Recall in the near future.
