DePuy Hip Replacement - DePuy ASR and Corail Hip System

Claudine Q. Homolash - Product Liability Attorney
(215) 790-7379
Advances in medicine now enable people with joint problems to replace their diseased cartilage and bone with artificial prostheses. One of the most common replacement surgeries is the hip implant, which allows patients to maintain reasonably active lifestyles without the pain that is often associated with a degenerative hip. Of the many companies that manufacture joint replacement components, Johnson and Johnson, parent company of DePuy Orthopaedics, Inc., has recently been in the news for a recall issued in July for its DePuy ASR system, and for marketing the Corail Hip System using illegal methods.

A DePuy ASR hip recall was issued in July, 2010 due to a high failure rate of the metal-on-metal hip implants. A number of lawsuits have been filed by individuals who have experienced problems and complications after receiving DePuy hip replacement products. Patients who had the system implanted may suffer when metal particles shed into the body from the metal-on-metal design. The particles can cause soft tissue damage, inflammatory reactions, and bone loss. Between 2007 and 2009, more than 500 patients reported problems with their hip replacement devices. To resolve the problem, patients may need to have the devices replaced, and treatment for additional surgeries, inflammation, bone loss and soft tissue damage can be extensive.

The FDA issued a warning letter to DePuy Orthopaedics, Inc. president David Floyd on August 19, 2010, ordering the company to halt marketing the Corail Hip System. The Corail system was approved under the FDA's premarket approval system, an expedited process that requires medical devices to be functionally equivalent to devices already on the market in order to fast-track the approval process. However, according to the warning letter, DePuy's brochure about the device lists a number of claims that were never approved by federal regulators.

If you have received a hip implant in the last few years, you should contact your doctor to determine the model of your implant. This should be done even if you are not presently experiencing any negative side effects because serious problems could arise at any time. If it turns out that you are in fact depending on a potentially defective hip implant, you should take action to protect your rights. Contact Claudine Homolash at (215) 790-7379 so I can help you pursue financial compensation for the pain, suffering, and medical costs that you have sustained as a result of these unsafe hip replacement devices.

While medical technology has helped relieve the suffering of many people, the Institute of Medicine estimates that almost 1.3 million Americans are injured or die as the result of faulty medical products. Claudine Homolash, Esq. represents the injured victims and families of those who have died because the makers and suppliers of medical devices failed in the design, marketing promises, or the manufacturing of their products. If you experienced any problems after receiving a DePuy hip replacement, it is important that you immediately contact a qualified personal injury attorney who is familiar with product liability claims and the tactics of corporations and insurance companies. Call the experienced lawyer, Claudine Homolash at (215) 790-7379.
If you hesitate to file suit within the specified time limit, you may lose your opportunity forever.

DePuy ASR Hip Replacement Recall - CALL ME AT 215-790-7379 or EMAIL ME AT chomolash@sheller.com

DePuy has issued a recall for its ASR hip implants that will affect thousands of patients. If you've been harmed by the DePuy ASR hip replacement recall, filing a hip replacement lawsuit to seek compensation for your injuries is your right.
ASR hip replacement systems are the subject of a recall by manufacturer DePuy Orthopedics. DePuy ASR hip replacements have had an unusually high failure rate, and many people who have received DePuy hip replacements have had to undergo multiple, painful surgeries to replace the defective hip implant. If you've been harmed by a DePuy ASR hip replacement, it's your right to file a hip replacement recall lawsuit against DePuy and seek compensation for your injuries.

Do I Have Grounds for a Hip Replacement Lawsuit?
If you have received a DePuy ASR hip replacement since 2003 you may have grounds for a lawsuit against DePuy. The ASR hip replacements have an unusually high failure rate and can become loose and fracture the bone around the implant, the implant's ball and socket can become dislocated, and metal from the implant can even flake off and enter the bloodstream. Orthopedic specialists have been calling attention to the high failure rate of ASR hip replacements for years, and both DePuy and its parent company Johnson & Johnson have been warned by the FDA numerous times about defective products.

If you or a loved one received a hip replacement anytime after 2003 and has had any pain or complications resulting therefrom, please email or call Claudine Homolash at chomolash@sheller.com or 215-790-7379 for a free consultation.

Zimmer Durom Hip Implant Recall

On July 24, 2008, Zimmer Holdings, the nation's largest producer of orthopedic devices, announced the suspension of sales of an artificial hip implant component due to a high failure rate. The medical device, a hip socket known as the Durom cup, was first sold in the U.S. in 2006 and has been implanted in 12,000 patients.

Physicians have complained that device is faulty with possibly hundreds of patients needing replacement surgery in the coming years. Zimmer has denied that the Durom hip implant is defective. Instead, Zimmer claims surgeons have failed to implant the device properly and was suspending its sale to provide doctors specialized training for the implant surgery.

Not all physicians have agreed with Zimmer's assessment. In April 2008, Dr. Lawrence Dorr, an orthopedic surgeon in Los Angeles, California, publicly warned other orthopedists about cup failures his patients were experiencing. When questioned on Zimmer's announcement, Dr. Dorr told the New York Times that he did not plan to start reusing it. "It is a bad design," he said.

The law in most states provides individuals with legal claims and the right to compensation for injuries they suffer as a result of a medical device that is defective or fails to perform as advertised. Patients may file a personal injury lawsuit seeking compensation for their pain and suffering, medical expenses including the cost of replacement surgery, lost past and future wages and punitive damages.

Claudine Homolash of Sheller, P.C. represents persons across America injured by defective and dangerous medical devices. Ms. Homolash can be reached at (215) 790-7300, or chomolash@sheller.com