800-401-4720
Dangerous Drugs
Injuries
Contact Us
Dangerous Drugs and Injuiries Attorneys
Dangerous Drugs and Injuries Lawyers Who We Are What We Do Frequently Asked Questions Contact Us
We Sue Companies That Sell Dangerous Drugs
Nationwide Law Practice click here to be instantly connected to our office Medical and Legal News
DePuy ASR Hip Implant

DePuy ASR Hip Replacement Recall Lawsuits

On August 24, 2010, Johnson & Johnson subsidiary DePuy Orthopaedics, Inc. announced the recall of the DePuy ASR XL Acetabular System hip replacement implant.  If you or a loved one received this implant, surgery will likely be necessary to remove and replace the device (revision surgery).  Any person who received the DePuy ASR should seek legal counsel -- otherwise you risk being shortchanged for your injuries by corporate giant Johnson & Johnson.

The DePuy ASR Hip Replacement Defect

DePuy ASR Metal Wear The DePuy ASR XL Acetabular System is a metal-on-metal total hip replacement device.  It was used for hip replacement surgeries beginning in July 2005 until early 2010, but is now off the market.  It was implanted in approximately 93,000 patients.

Johnson & Johnson defectively designed the DePuy ASR hip system by providing insufficient coverage of the cup resulting in the forces of the ball against the cup over concentrating at a particular spot (usually the edge of the cup). The DePuy ASR defect causes a variety of problems, which ultimately require revision surgery:

  • Loosening of the Hip Implant: the implant does not stay attached to the bone in the proper position.
  • Dislocation of the DePuy ASR: where two parts of the implant that move against each other are no longer aligned.
  • Fracture of the Hip Bone: the bone to which the implant is attached breaks.
  • Release of Metal Ions into the Body: Metal-on-metal implants cause metal particles to be shed into the body and the implants to wear down. The metal particles can damage the tissue and bone around the implant, causing loosening of the hip.

Determining Whether Your DePuy ASR Hip Replacement is Injuring You

DePuy Implant Injury Everyone who received a DePuy ASR hip implant should be tested for disease-causing cobalt and chromium metal ions in their blood. Release of these metal ions into the body is a result of the ASR's metal-on-metal design. These metal ions may be injuring you even if you don't have any outward symptoms. It is extremely important to determine whether this is happening to you early, because early revision of poorly performing hip replacements in these circumstances improves the chances of success of your revision surgery.



For those who received the DePuy ASR who do experience symptoms, these are the most common:
  • Difficulty walking
  • Hip pain
  • Thigh or groin pain
  • Pain when rising from a seated position
  • Pain when walking or bearing weight
  • High levels of microscopic metal particles around the hip (this is determined by a blood test)
  • Dislocation of the implant
  • Swelling
Importantly, as outlined above, even if you don't have these symptoms, the DePuy ASR still may be harming you and/or ultimately will need to be replaced.

DePuy ASR Hip Implant Litigation

If your hip replacement surgery or that of your loved one used a DePuy ASR XL Acetabular System, the attorneys at DeCarli Law can help you. Johnson & Johnson should be held accountable for the injuries caused by its defective product because they knew of the defects in the DePuy ASR, yet continued to sell it. Furthermore, even though Johnson & Johnson might claim it will compensate you for your injuries, without a lawyer fighting for your interests, you risk signing away your rights without receiving the compensation you deserve. Contact DeCarli Law for a free, confidential, no-obligation telephone consultation.

Attorney Web Design The information on this website is for general information purposes only. Nothing on this or associated pages, documents, comments, answers, emails, or other communications should be taken as legal advice for any individual case or situation. The information on this website is not intended to create, and receipt or viewing of this information does not constitute, an attorney-client relationship. DeCarli Law only represents individuals pursuant to a signed, written contract.

Address: 50 California Street, Suite 1500 San Francisco CA 94111 Toll Free: 1-800-401-4720 Phone: 1-415-738-6144
Debra DeCarli and Bob DeCarli are licensed by the State Bar of Texas and the State Bar of California.

DeCarli Law represents drug side effects and defective medical devices personal injury clients for claims, lawsuits and settlements in Alabama AL, Alaska AK, Arizona AZ, Arkansas AR, California CA, Colorado CO, Connecticut CT, Delaware DE, Georgia GA, Hawaii HI, Idaho ID, Illinois IL, Kansas KS, Maine ME, Maryland MD, Massachusetts MS, Minnesota MN, Mississippi MS, Montana MT, Nebraska NE, New Hampshire NH, New Jersey NJ, New Mexico NM, New York NY, North Carolina NC, North Dakota ND, Oklahoma OK, Oregon OR, Rhode Island RI, South Carolina SC, South Dakota SD, Tennessee TN, Utah UT, Vermont VT, Virginia VA, Washington WA, Washington D.C, West Virginia WV, Wisconsin WI and Wyoming WY. The attorneys of DeCarli Law are licensed in California and Texas. DeCarli Law's practice includes lawsuits for Propecia side effects, Finasteride lawsuits, Topamax lawsuits, Fosamax lawsuits, Gadolinium lawsuits, NSF lawsuits, Nephrogenic Systemic Fibrosis Lawsuits, YAZ lawsuits, Yasmin lawsuits, Ocella lawsuits, and Zarah lawsuits.