The recalls began in 2010 when those that had received the implants received a notice from their surgeons that the DePuy ASR XL Acetabular System that was implanted had been recalled by the manufacturer.
Approximately five years after the hip implants, 1 in 8 patients had to have some kind of revision performed. Revisions at this point after implantation are not typical in hip replacements. The recall had to be done because the device needed to be tested and monitored more to ensure proper functionality. If you have received one of these hip replacement devices, you may need to have more surgery. You also need to contact your Minnesota DePuy hip replacement attorney regarding the pain and suffering you have experienced.