Posts Tagged ‘Hip Recalls’

2011 Report – British Doctors Find 49% Failure Rate in Depuy Hip Implants

Wednesday, March 23rd, 2011

According to recent data in the United Kingdom, the Depuy ASR hip implant is failing at a rate of 49%.  The rate is four times higher than Johnson & Johnson’s orthopaedic division had indicated last year when it recalled the faulty hip implant.

Bloomberg News reports:

“The British Orthopaedic Association and the British Hip Society said in a statement this week that data on the ASR XL Acetabular System from four surgeons show the rate of second operations, or revisions, ranges from 21 percent after four years to 49 percent after six years.”
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Number of Americans with Defective Depuy ASR Hip Implants Expected to Go Up

Friday, March 18th, 2011

In August of last year, Depuy Orthopaedics was forced to recall its ASR hip implant.  The faulty implant was on the American market for fewer than 5 years, but long enough to cause serious harm to the patients who underwent hip surgery with the defective ASR hip replacement.

 

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Depuy President Steps Down After Recall of Faulty Hip Implants

Wednesday, March 16th, 2011

According to a recent Bloomberg news report, David Floyd has officially stepped down as world president of DePuy Orthopaedics.  Depuy is the division of Johnson & Johnson that produces artificial hip and knee replacements.

Floyd’s resignation comes amid continuing controversy about Depuy’s recall of its ASR hip implants.  The New York Times recently reported that the ASR hip implants have been “failing worldwide at unusually high rates after just a few years.”  Depuy’s faulty hip replacements have caused many patients to undergo painful revision surgery.

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Update: DePuy Recalls Defective A.S.R. Hip Implant, But High Failure Rates Continue

Friday, February 4th, 2011

Depuy ASR Hip RecallThis past December 2010, the New York Times reported that Johnson & Johnson’s DePuy A.S.R. hip implants have been “failing worldwide at unusually high rates after just a few years.”Despite being promoted as a breakthrough in hip replacements, the faulty DePuy A.S.R. (which stands for Articular Surface Replacement) is now being called “one of the most troubled orthopedic implants of the past decade.”

Although evidence of the defective A.S.R. hip implant had been mounting for years, DePuy Orthopaedics, a division of Johnson & Johnson and the world’s leading manufacturer of hip implants, has continued to claim that there were no problems with the troubled A.S.R.  (more…)

Recent Hip, Knee, and Replacement Joint News

Monday, May 3rd, 2010

4/13/2009

Defective joint and product liability lawyers, Keefe Bartels & Clark have begun investigation of Wright Medical Technology Total Hip Implants

The defective joint implant attorneys at Keefe Bartels & Clark have begun investigating reports regarding total hip implants manufactured by Wright Medical Technology, Inc., a Tennessee Corporation. Wright manufactures and distributes orthopaedic implants including implants for the hips and knees. The FDA’s Manufacturer and User Facility Device Experience Database (MAUDE) indicates several reports regarding the failure of Wright Total Hip Systems that use the Conserve product line as well as the Profemur Product lines.

The defective product attorneys at Keefe Bartels & Clark are currently screening patients who had the Conserve Plus Cup and the Profemur Stem and/or Neck implants utilized in their total hip replacement and are experiencing problems or have experienced a device failure. In some cases, these components fracture, resulting in a “catastrophic” failure of the hip implant device. Other components may not promote, and may in fact, retard, bony ingrowth, resulting in the devices loosening and requiring additional surgery to repair or replace the failed component. These implants may have been designed or manufactured in a defective manner. If you believe you may have one of these hip implant components, and are suffering from pain, swelling, or limitation on your range of motion, or if you have had to have the hip implant revised, please contact the defective hip implant lawyers at Keefe Bartels & Clark immediately.

1/22/2009

New Jersey Court Announces Application for Mass Tort Designation of Litigation involving Stryker Trident Hip Implants and assignment for centralized management in Atlantic County, New Jersey.

Motion made for Mass Tort designation for Stryker Trident Hip System

Pursuant to New Jersey Court Rule 4:38A and the Revised Mass Tort Guidelines, application has been made to the New Jersey Supreme Court requesting that the claims made against Stryker Corp., and its subsidiary Howmedica Osteonics Corp., regarding the Stryker Trident Hip Implant System be designated a Mass Tort and sent to Judge Higbee in Atlantic County New Jersey for centralized management.

The Stryker Trident Hip Implant is a ceramic implant that has been the subject of numerous claims involving the hip implant making squeaking noises. This sound is caused by the high levels of friction at the acetabular interface of the implant. This condition can be an indicator of more serious problems with the implant in the future, and the hip implant attorneys at Keefe Bartels & Clark allege that these devices suffer from either a manufacturing or design defect which is resulting in the squeaking hip noise reported by some patients. If you or a loved one has a hip implant that is squeaking, please contact our office immediately.

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