DePuy Hip Replacement Recall

Johnson & Johnson’s artificial joint replacement company, DePuy Orthopaedics, Inc. has issued a recall of two hip replacement products because of higher failure rates that necessitated second surgeries.

DePuy recalled the ASR Hip Resurfacing System and the ASR XL Acetabular System after data showed that within five years, one in eight patients needed a “revision surgery,” which is required when an artificial joint doesn’t properly fit. Serious pain and difficulty walking can result from a faulty hip replacement.

The hip implant recall affects an estimated 93,000 replacement systems and more than 29 different models of hip replacement implants.

What Hip Replacement Products Have Been Recalled?

DePuy has recalled the following hip replacement products:

  • ASR Hip Resurfacing System
  • ASR XL Acetabular System

According to The Associated Press, the ASR XL has been on the market since 2004 and was sold worldwide. The ASR Hip Resurfacing System has been on the market since 2003 and was exclusively available outside the United States.

All remaining products on hospital shelves will be immediately removed.

How Can I Tell if I Have a Recalled Hip Device?

DePuy suggests contacting your orthopaedic surgeon to determine if your hip implant has been recalled. If you don’t know who performed your hip replacement surgery, ask your primary care physician or someone at the hospital where the surgery took place.

What Is Total Joint Replacement?

Total joint replacement (TJR), also known as arthroplasty, utilizes modern polymers and metals combined with advanced techniques to create artificial joints capable of mimicking the natural actions of the human body while alleviating the extreme pain caused by musculoskeletal conditions such as hip damage caused by a serious injury or by conditions such as rheumatoid arthritis.

Serious injury and aging are the main causes necessitating joint replacement procedures. There are more than half a million of these procedures performed every year. Musculoskeletal conditions are the most common worldwide cause of severe, long-term pain and physical disability, accounting for $254 billion in medical expenditures in the United States every year.

What Should I Do if I Received a Defective Hip Replacement Component?

Always consult your doctor or physician regarding health-related issues, but if you or someone you care about received defective joint replacement components and had to have another surgery to correct this condition, we would like to speak with you right away. Call us or fill out a free online consultation form for an immediate evaluation of your case.

This law firm is not affiliated with, sponsored by, or associated with The Associated Press, DePuy Orthopaedics, Inc., or Johnson & Johnson.

Free Initial Consultation

If you have been injured by a replacement hip from DePuy, contact a defective medical device lawyer at Stewart & Stewart Attorneys. Our Indiana defective product lawyers represent victims throughout the state, including Carmel, Indianapolis, and Anderson. We have also successfully advocated for clients throughout the area, including Fort Wayne, Gary, Indianapolis, and South Bend. Complete a free online consultation form or call us at (800) 33-33-LAW!

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