DePuy Orthopedic Hip Replacement Recalls
Johnson & Johnson, along with its subsidiary DePuy Orthopaedics, have announced a recall of two acetyabular cups hip replacement systems due to a high rate of failures and new data showing one in eight patients requires secondary hip replacement.
Every year, thousands of successful hip replacements are performed, bringing a better life to men and women around the world. Unfortunately, this was not the case for patients who received a defective design following hip replacement surgery using either DePuy’s ASR Hip Resurfacing System™ or the ASR XL Acetabular Cups System™.
Ten of thousands of patients worldwide have received the faulty replacement device. Data compiled by the National Joint Registry (NJR) of England and Wales reveals that a full 13% required additional surgery within five years. For this reason, it is strongly recommended that surgeons monitor hip replacement patients closely and perform evaluations as needed to ensure patient safety and comfort.
The recalled DePuy Orthopaedics ASR Hip Resurfacing System is a partial hip replacement system which uses a metal cap placed on the ball of the femur. Also involved in the recall is the ASR XL Acetabular System, a traditional hip replacement system. Both systems use a metal-on-metal design which was discontinued by the manufacturer in 2009. The primary issue is that, as the metal parts move together, metal debris is shed into the patient’s body, leading to pain, immobilization, inflammation, bone loss and other health concerns. Other potential issues include loosening of the cup and detachment from the bone, dislocation, and fractures.
If you or a family member believe you are a victim of defective artificial hip and would like to discuss your legal options with a Sacramento Defective Product Attorney, contact me online - or call me at 916.921.6400 to set up a FREE consultation.