The OtisKnee device, made by OtisMed Corporation, was not approved by the Food and Drug Administration (FDA) to be used in knee replacement surgeries. The OtisKnee devices were not proven to be safe or effective. OtisMed Corporation distributed and marketed...
Read MoreHurley McKenna & Mertz, P.C. recently filed lawsuits in federal court on behalf of seven individuals who received defective Stryker hip implants. In July 2012, Stryker issued a voluntary worldwide recall of its Rejuvenate and ABG II hip implants. Studies...
Read MoreNBC TV interviews Chris Hurley and Mark Stephan about Stryker Defective Hip Lawsuit from Christopher Hurley on Vimeo. In 2007, Mark Stephan suffered catastrophic injuries when his front wheel unexpectedly disengaged from his bicycle. This crash paralyzed Mark from the...
Read MoreIn the wake of an FDA investigation of metal-on-metal hip implants, Stryker recently followed the lead of other artificial hip manufacturers and recalled its Rejuvenate Modular and ABG II modular-neck hip stems. According to Stryker, these components are dangerous because...
Read MoreAfter reading the article “In Medicine, New Isn't Always Improved” in the New York Times last Sunday, I am struck by how many recipients of metal-on-metal hip implants might be affected by the faulty design and poor testing of the...
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