Zimmer Hip Implant Recall
On July 24, 2008, Zimmer Holdings, the nation's largest producer of orthopedic devices, suspended all U.S. sales of an artificial hip implant component, known as the ?Durom cup,? due to a high failure rate. Zimmer has sold nearly 12,000 of the implants in the United States since 2006. In April 2008, Dr. Lawrence Dorr, an orthopedic surgeon in Los Angeles, California, publicly warned other orthopedists about the high number of cup failures his patients were experiencing. Dr. Dorr told the New York Times in a July 24, 2008 interview that he did not plan to start reusing it. "It is a bad design," he said. While Zimmer denies the device is defective, in a letter to orthopedic surgeons dated July 22, 2008, it acknowledged that some patients receiving the artificial hip implant may require revision surgery. Critics of the device fear that hundreds of patients may require implant replacement.
Questions and Consultations
If you or someone you love received a Zimmer Durom Cup artificial hip implant after March 16, 2006, and you would like to discuss your rights, please complete our brief evaluation form. A member of Seeger Weiss LLP's experienced staff will call you to discuss your potential claim. Attorney consultations incur no obligation on your part and all initial consultations are free of charge and do not create an attorney-client relationship. Seeger Weiss LLP has office locations in New York, New Jersey, Pennsylvania, and Oklahoma and its attorneys practice in courts throughout the country.
Link To Lawyer Seek's Zimmer Hip Implant Recall Content:
<a href='http://www.lawyerseek.com/Practice/Pharmaceutical-Injury-C1/Zimmer-Hip-Implant-Recall-P192/'>Zimmer Hip Implant Recall: Lawyer Seek</a> |
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