If you underwent a hip replacement surgery after July 2003 with the DePuy Orthopaedics ASR XL Acetabular System (total hip replacement) or the ASR Hip Resurfacing System (hip resurfacing), you may be among the estimated 93,000 patients who have a potential claim against the manufacturer for damages.

The Brad Hendricks Law Firm wants to help if you or a loved one has been harmed by these products marketed by DePuy Orthopedics, a subsidiary of Johnson & Johnson.

The ASR hip replacement system was approved by the United States Food and Drug Administration (“the FDA”) in 2005. At that time, the devices were given a 501(k) approval by the FDA. In other words, the devices were approved under the belief that they were “substantially similar” to other hip replacement devices on the market. Accordingly, the DePuy systems were approved without going through more arduous clinical trials.

Touted as a “high performance” replacement system with significant advantages over other brands of implants, DePuy claimed its metal-on-metal implant system had an estimated life of approximately fifteen years. However, on August 26, 2010, DePuy issued a worldwide recall of its ASR XL Acetabular and ASR Hip Resurfacing systems, citing a failure rate exceeding 12 percent after only five years. Some expect this failure rate to increase dramatically as the problems with the systems become more widely reported.

DePuy had previously halted all sales of these systems in late 2009, denying that its decision was related to reported failures; however, since 2008, the FDA has received an estimated five hundred complaints regarding the premature failure of the implants. Unfortunately, this recall comes much too late for those patients who were sold the devices, many of whom reported the following problems:

  • Loosening, where the implant failed to stay attached to the bone in the proper position;
  • Fractures, where the bone around the implant may have broken; and
  • Dislocations, where the two parts of the implant that move against each other are no longer aligned.

Problems occur across all hip sizes, although a higher percentage of defective hips have smaller heads, which are usually used in women. Those impacted by the premature failure of the devices face considerable physical, emotional, and financial adversity through no fault of their own.

Recent developments in the medical literature indicate that many metal-on-metal implants are defective. A recent study indicated that up to 50 percent of patients with a metal-on-metal implant may be forced to undergo revision surgery within six years of receiving the implant.

These implants are defective and fail due to a design flaw for two principle reasons. First, the device slips or the shell does not sit in place in the hip, and it resists bone growth. Second, the friction of the metal-on-metal (metal hip ball and metal hip socket) causes microscopic shavings and metal debris to be released into the surrounding tissue and blood. This can lead to a painful, inflammatory reaction in the tissue and high blood metal content. For these reasons, our firm is expanding representation to include other metal-on-metal hip implants.

Many doctors are recommending that patients with a metal-on-metal implant undergo blood testing to determine whether their patient has high levels of cobalt or chromium in the patient’s bloodstream. You may want to consider asking your doctor to perform such blood tests.

If you have received a hip implant since 2003, or if you have been advised to undergo an additional hip replacement surgery, you should contact your doctor immediately to determine which hip replacement device was initially implanted, even if you are currently experiencing no adverse symptoms or side effects. Complications from these devices can occur at any time.

If you have a DePuy hip replacement implant, you should not have to suffer because of DePuy’s failure to release information about the problems in its hip replacement systems. You or a loved one may be entitled to compensation.

For a free consultation about your claim, please contact The Brad Hendricks Law Firm today at (501) 214-0998 or (870) 330-0475.

The notice letter provided to physicians suggests only pre-2011 femoral heads are at issue. However, there are clearly cases where there is corrosion with heads after 2011, making it more important than ever for patients to seek care immediately before it is too late.

If you or a loved one have a metal-on-metal hip replacement implant and believe it was manufactured by Stryker® Orthopaedics, please call The Brad Hendricks Law Firm today to discuss your rights and potential claim at (501) 214-0998 or toll-free at (870) 330-0475.

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The Brad Hendricks Law Firm proudly serves clients throughout Arkansas, including Arkadelphia, Benton, Conway, El Dorado, Fayetteville, Fort Smith, Hot Springs, Jonesboro, Little Rock, Pine Bluff, Texarkana, and West Memphis as well as numerous counties throughout the State of Arkansas, including Arkansas County, Baxter County, Benton County, Bradley County, Calhoun County, Clark County, Columbia County, Conway County, Crittenden County, Faulkner County, Garland County, Hempstead County, Hot Spring County, Izard County, Lawrence County, Lonoke County, Monroe County, Nevada County, Pike County, Poinsett County, Polk County, Pope County, Prairie County, Pulaski County, Saline County, Sharp County, Stone County, Washington County, White County, Woodruff County, and Yell County, and all other counties in the State of Arkansas.

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