YourLawyer.com® 1-800-LAW-INFO (1-800-529-4636)

Zimmer Durom Cup


AddThis Social Bookmark Button

Zimmer Durom Cup Hip Implant Injury Lawyers

Keywords: Durom Hip Implant Lawyer Problems Attorney Failure Lawsuit

The lawyers and attorneys at our firm are offering free case evaluations to individuals injured by defective ZImmer Durom Cup hip implant components.  In July 2008, Zimmer Holdings announced it was suspending sales of the Durom Cup hip implant component due to a high number of patient complaints.  If you or a loved one has been injured by this defective device, we urge you to contact one of our Durom Cup hip implant injury lawyers as soon as possible to discuss your case.

The Durom Cup has been implanted in over 12,000 patients since it was first sold in the United States in 2006. The Durom Acetabular Component is a monoblock cup made of cobal chromium alloy, which is made from a single piece of material. It is designed for use in combination with Zimmer’s Metasul Metal-on-Metal Tribological Solution LDH (Large Diameter Heads). 

The Durom Cup was designed  for use in young, active patients who are likely to outlive a conventional hip prosthesis.  Unfortunately,  it has been alleged that patients implanted with this devie  often experienced crippling pain following surgery, leaving them more disabled than they had been before their hip replacement. Because of such problems, a  large percentage of patients receiving the Durom Cup may need to undergo additional surgery to have this allegedly defective component replaced.

Zimmer Ignored Durom Cup Complaints

Possible problems with the Durom Cup hip implant first became apparent in April 2008, when Los Angeles surgeon Dr. Lawrence Dorr publicly warned other orthopedists about cup failures his patients were experiencing.  According to Dr. Dorr - who was also a highly paid consultant for Zimmer - months after routine hip replacements, patients who had expected to live without pain were in agony.

After informing colleagues in a professional society about his experience with the Durom Cup, Dr. Dorr heard from several other doctors who reported similar problems.  The Durom Cup hip implant injury lawyers at our firm have also heard from numerous people about the crippling pain they experienced following their implantation with this defective device.

According to Dr. Dorr and other physicians, x-rays of patients who received defective Durom Cups showed that the socket was separating from bone, rather than fusing with it. For patients, who had been told their new hips might last 15 to 20 years, it meant agony as the metal cup moved around in the hip socket and rubbed against bone.   Such crippling injuries are devastating, and many Durom cup recipients reported that they were in much worse shape after their surgery than before. 

In early 2008, Dr. Dorr reported his concerns about the Durom Cup to executives at Zimmer.   The doctor said  his complaints fell on deaf ears.   Zimmer actually had the audacity to blame Dr. Dorr's surgical techniques for the problems his patients experienced.  At the time, Zimmer did nothing to address his concerns.

It is odd that Zimmer would blame Dr. Dorr's skills for the Dorum Cup problems his patients experienced, given that the surgeon was a company consultant.  What's more, Dr. Dorr is a veteran of more than 5,000 hip replacement surgeries.  At 67, he has been performing these operations for decades. 

Zimmer's alleged attempts to blame Dr. Dorr for failures caused by ithis device indicate that the company may have been more interested in protecting its own bottom line than patient well-being.  It is the intention of our Durom Cup hip implant lawyers to hold Zimmer accountable for this negligence.

Zimmer Finally Suspends Sales of Durom Cup

In April 2008, after being rebuffed by Zimmer, Dr. Dorr took his concerns to the American Association of Hip and Knee Surgeons. In late May, Zimmer finally informed surgeons that it was investigating Dr. Dorr’s complaint but that it did not suspend sales, as the doctor had recommended.  While it investigated complaints, roughly 1300 more patients were implanted with the Durom Cup in the U.S.

According to Zimmer's own investigation, some clinics using the Durom Cup experienced failure rates as high as 5.7%.  In spite of the evidence that something was amiss with the design of the Durom Cup, Zimmer is still blaming doctors for its high failure rate.  Our Durom Cup hip implant injury lawyers find it difficult to believe that so many surgeons could be making the very same mistakes that have led to hundreds of similar patient complaints and injuries. 

Despite its contention that the Durom Cup implant is safe, Zimmer has stopped marketing the device in the U.S.  The company has also stopped the enrollment of an investigational clinical trial evaluating Durom in hip resurfacing procedures.  Zimmer, however, will not give up on the Durom Cup.   The company plans  to update the labeling for the device, and reintroduce to the U.S. market by 2009.

Legal Help for Durom Cup Hip Implant Victims

If you or a loved one has experienced crippling pain or injury following implantation with the Zimmer Durom Cup hip implant component, you have valuable legal rights.  Please fill out our online form, or call 1-800-LAW-INFO (1-800-529-4636) to discuss your case with an experienced Durom Cup hip implant lawyer.

Zimmer Durom CupRSS Feed

Orthopedic Docs Withheld Info About Industry Pay When Presenting Research

Oct 8, 2009 | Parker Waichman Alonso LLP
A new study has found that doctors who presented research  last year at the annual meeting of the American Academy of Orthopaedic Surgeons weren't always as forthcoming as they should  have been about their financial relationships with the manufacturers of artificial joints.  The study appears this week in The New England Journal of Medicine.The financial relationships between  the medical industry and doctors have caused controversy in recent years.  In 2007, a U.S....

Kickback Charges Against Orthopedic Device Makers Dropped

Mar 31, 2009 | Parker Waichman Alonso LLP
Criminal charges were dismissed yesterday against several orthopedic device makers because they have fulfilled the terms of deferred prosecution agreements they reached with U.S. prosecutors a year and half ago.  According to Dow Jones News Wire, Zimmer Holdings Inc., Johnson & Johnson unit DePuy, Smith & Nephew PLC and Biomet Inc. had all been accused of violating federal anti-kick back laws.According to Bloomberg News, the four companies  supply 95 percent of hips and knees...

Women Having Problems with Hip Device

Nov 11, 2008 | Parker Waichman Alonso LLP
Medical researchers internationally are concerned about the use of hip resurfacing techniques being used in women.  Regardless, hip implant device makers and some American doctors have aggressively promoted hip resurfacing, since it became available in the U.S. in 2006, several years after it went into use overseas.Hip resurfacing is targeted to physically active, middle-age patients, who are expected to outlive the normal 15-to-20-year life span of a full replacement joint.  The...

Payments to Joint Implant Doctors Continue

Oct 30, 2008 | Parker Waichman Alonso LLP
About one million Americans will undergo joint replacement surgery in the next year.  Given that, consumers might be interested to know how much money their orthopedic surgeon might be receiving from joint replacement makers.  Although some physicians may not receive funding for using a specific maker’s device, some could receive kickbacks as large as a million dollars, despite that a recent federal anti-kickback case targeted such questionable payments.Beginning in September...

Lifespan and Success of Artificial Hip, Knee Implants Unpredictable

Oct 7, 2008 | Parker Waichman Alonso LLP
A surprising number of people who receive artificial hips and knees will need to have their joints replaced, according to a recently-released study.  What's more, another study has found that there is no way to predict what kind of activities might put too much wear and tear on a new hip or knee implant.Knee and hip replacement surgery has become wildly popular.  According to the Associated Press, Americans undergo 478,000 knee replacements and 234,000 hip replacements every...

More Zimmer Durom Cup News

Defective Medical Devices
* Denotes required field.

Title

* First Name

* Last Name

* Email Address

* Phone Number

Cell Phone Number

Office Phone Number

Street Address

Apartment/Suite

City

State

Zip Code

Please provide the best method and times to contact you:

Date of birth of person injured
(mm-dd-yyyy):

Date of when you started using Device (MM-DD-YYYY):

Please describe any problems or injuries caused by the device:

Other Info:

No Yes, I agree to the Parker Waichman Alonso LLP disclaimers.Click here to review all.

Yes, I would like to receive the Parker Waichman Alonso LLP monthly newsletter, InjuryAlert.

please do not fill out the field below.

Home | Defective Drugs | Medical Devices | Toxic Substances | Accidents | Product Liability | Malpractice | Diseases
Nursing Home Negligence | Food Poisoning | Other Topics | Contact
Statement of Clients' Rights | Site Map | Vioxx | Mesothelioma | Permax | Dostinex | Composix Kugel Mesh X Large Patch
Ortho Evra | Fosamax | Fusarium Keratitis | Stevens Johnson Syndrome

© 2002-2010 YourLawyer.com®. All Rights Reserved.

Please note that you are not considered a client until you have signed a retainer agreement and your case has been accepted by us.
Prior results do not guarantee or predict a similar outcome with respect to any future matter.
Attorney Advertising