Defective Hips Used If you have gone through a hip replacement surgery in the last few years and are experiencing pain it may be due to a defective product. If you are suffering from any of the common warning signs please contact the experienced hip recall professionals at Kane & Silverman toll free at 866-484-6992. Our hip recall and replacement attorneys are here to help.
Your Hip may be Recalled If you are experiencing any pain or discomfort in your replacement hip since surgery, there is a good chance it may have been recalled. To learn more about recent hip recalls and faq's please contact the experienced hip recall professionals at Kane & Silverman toll free at 866-484-6992. Our hip recall and replacement attorneys are here to help.
Depuy & Zimmer Recall Over the last ten or so years three of the largest hip replacement manufacturers in the United States have had products recalled; Depuy, Zimmer and Stryker. If you would like to speak with a hip recall attorney please contact the experienced hip injury and recall professionals at Kane & Silverman toll free at 866-484-6992.
Kane and Silverman Howard Silverman has been practicing law for over twenty years. He has been selected as a Super Lawyer every year since 2008 and is a lifetime member of both the Million Dollar Advocates Forum and Multi-Million Dollar Advocates Forum. For free legal advice regarding your hip implant recall case, please contact Kane & Silverman toll free at 866-484-6992.
In January 2008 Stryker Corp recalled the Trident Acetabular PSL Cup and the Trident Hemispherical Cup following a discovery by the United Stated Food and Drug Administration of substandard, unsanitary conditions at two manufacturing plants as well as multiple reports of pain and injuries by patients. The first manufacturing facility located in Mahwah, New Jersey contained staphylococcus bacteria, rhodococcus spp, corynebacterium propin quum and other disease causing germs. A second facility, located in Cork, Ireland, had problems with product testing procedures.
Patients reported pain, broken parts, migrating of parts, loosening of hip cups, squeaking, grinding, and crunching while walking. The first sign of trouble came in January of 2005 when several patients complained of pain. Two years later the FDA would spend six weeks inspecting the Manwah, New Jersey facility and found deficiencies in the quality control stages of manufacturing as well as the previously mentioned presence of germs.
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