At issue is the high rate of repeat total hip replacement (THR) surgeries needed by people who have received the parts. An estimated 93,000 people will be affected by Johnson & Johnsons latest product recall.
Affected hip replacement parts involved in the recall include the DePuy ASR XL Acetabular System, which is the cup portion of a replacement hip joint, and the DePuy ASR Hip Resurfacing System. The high failure rate has been attributed to the design of the hip components. Small pieces of metal are released into surrounding tissue, preventing the device from bonding firmly with natural bone. Individuals with this device still in them will need to be monitored closely and ultimately may need hip revision surgery.
Although this recall is voluntary, DePuy also received a warning letter from the FDA that charges the company is marketing some other joint replacement products without required approval.
Patients who reported problems in the first five years and had revision surgery reported a variety of symptoms, including pain, swelling and problems walking. These symptoms are normal for patients following a hip replacement, but can be a sign that something is wrong if they continue or come back frequently. These symptoms may indicate serious problems, including:
Loosening when the implant does not stay attached to the bone in the correct position
Fracture where the bone around the implant may have broken
Dislocation where the two parts of the implant that move against each other are no longer aligned
Metal-on-metal modular hip implant devices have the advantage of a lower wear rate and lower chances of dislocation. But, the wear of metal parts against each other, corrosion, generates metallic debris that makes its way into the blood stream and ultimately to muscle, bones and organs. High levels of metals, predominantly cobalt, chromium and molybdenum, can result in metallosis or periprosthetic osteolysis ‘ the degeneration of bone due to infection.
Symptoms can start with hip and joint pain and can include tinnitus, vertigo, deafness, blindness, headaches, peripheral neuropathy and heart and thyroid issues.
The following products are all currently being investigated:
Metal-on-metal
DePuy ASR
DePuy Pinnacle
Wright Dynasty
Wright Conserve
Biomet M2a
Zimmer Durom Cup
Smith & Nephew R3
Failed Metal Taper/Stem Systems
Wright Profemur
Stryker Rejuvenate
Stryker ABG II
Stryker Accolade
Jeffrey A. Pitman
Mr. Pitman is a member of the Nursing Home Litigation Group of the American Association for Justice. Mr. Pitman was President of the Wisconsin Association for Justice in 2013 and is a current member of the National Academy of Elder Law Attorneys (NAELA). He lectures extensively on nursing home abuse and neglect and has authored numerous articles in the area of personal injury litigation.
DePuy Hip Replacement Recall Lawyer Near Me – Contact PKSD Today
If you suffered complications after receiving a DePuy implant in Milwaukee, Wisconsin, the DePuy hip replacement recall lawyers at PKSD can help you understand your legal options and pursue compensation. Contact us to tell us about your case – the consultation is free. PKSD helps victims in all of Wisconsin, and our firm is conveniently located near you. We have an office in 1110 N Doctor M.L.K. Jr Dr #320, Milwaukee, WI 53203. Call (414) 333-3333 to schedule your free case evaluation today.
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This page has been written, edited, and reviewed by a team of legal writers following our comprehensive editorial guidelines. This page was approved by attorney Jeffery A. Pitman, who has more than 28 years of legal experience and handled thousands of personal injury cases while obtaining millions of dollars in verdicts and settlements in Wisconsin.
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