Zimmer Durom Cup Artificial Hip
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Contact the Law Firm of Carabin & Shaw today, we are reviewing potential cases for individuals who know they received the hip implant component or suspect that may have and/or are suffering:
- Unexplained hip pain more than three months after hip replacement
- Loosening of their artificial hip implant
- Hip replacement revision surgery
The Zimmer Durom Acetabular Component is a relatively newer type and design of artificial hips. The Durom Hip was introduced in the United States in 2006. It is designed for use with Zimmer's Metasul Metal-on-Metal Tribological Solution Large Diameter Heads (LDH). Unlike traditional hip replacement components, the Zimmer Durom Cup is made from a single piece of materials.
In April 2008, prominent Los Angeles orthopedic surgeon, Dr. Larry Dorr, notified members of the American Association of Hip and Knee Surgeons about the Durom Cup, when Dr. Dorr was encountering with patients who received the component. Problems such as loosing of the components and a higher than expected rate of revisions were identified by Dr. Dorr.
After initially dismissing Dr. Dorr's report of problems, Zimmer agreed to initiate an investigation of the Durom Cup problems in May 2008. After reviewing data from over 3,100 cases, Zimmer concluded that the technology and design parameters of the Durom Cup require a higher degree of precision than was common in hip replacement surgical techniques in the United States and that additional instructions and training should be provided to doctors before the devices are implanted.
In July 2008, the manufacturer decided to suspend U.S. sales of the product, however the Durom Cup was not recalled since Zimmer is contending that it did not uncover evidence of any manufacturing defect or design defect. In fact, they intend to reintroduce the artificial hip implant after they develop instructions about the special surgical techniques that doctors need to use to avoid the risk of Durom Cup problems. They have also indicated that they will implement a new training program for U.S. surgeons.
Over 12,000 individuals across the United States have had a Zimmer Durom Cup implanted during their hip replacement surgery. Hundreds of these individuals, if not more are experiencing or could begin experiencing a loosening of the component and the need for additional surgeries which was caused by the negligence of Zimmer Holdings, Inc. It is our belief that Zimmer introduced this product without providing adequate warnings or instructions about the proper use and surgical techniques required.
The Carabin & Shaw Law Firm are now offering free case reviews for those who have experienced problems after their hip replacement. If you believe that you or a loved on are suffering from this medical product then call our Law Firm today for a free consultation and claim evaluation. There are no fees or expenses unless a recovery is obtained. Call us toll free at 1-800-862-1260.
TRADEMARK NOTICE: Durom is a trademark of Zimmer, Inc.
The Carabin & Shaw Law Firm, its' lawyers and this website is in no way affiliated with Zimmer, Inc. The use of this mark is solely for informational and product identification purposes.


