• Vena Cava IVC Filter Lawyers- IVC Filter Helpline:   Bard and Cook IVC Filter Lawyers Lawsuits are being filed  because the IVC (Inferior Vena Cava) Filters have been linked to migration and perforation of various organs in the body. An IVC (In...

  • Omni Life Hip Apex Arc Replacement Lawyers: Omni Life Apex ARC Hip Replacement Lawyers OMNI Life Science’s ARC hip Replacement has a  chromium and cobalt ball connecting to a titanium stem, is a metal-on-metal design. This hip replacement is l...

Posts Tagged ‘hip replacement recall’

DePuy Pinnacle Lawyers, DePuy Pinnacle Helpline

Written by lisaspitzer on . Posted in Depuy Hip Replacement Blog, Depuy Hip Replacement News, Stryker Hip Replacement, Stryker Hip Replacement Lawyer

DePuy Hip Replacement Helpline has launched a DePuy Pinnacle Helpline to locate all people with a faulty DePuy Pinnacle. You must file your DePuy Pinnacle lawsuit right away.

Recipients of the various metal on metal hip implants are suffering nationwide.

“I used to ski, hike and swim. Tennis was my favorite sport and I miss it so much. I can’t do any of that anymore. All I can do now is watch videos on the computer or watch TV. As you can imagine, I gained weight (I just went on a diet) since I had my hip replaced. I can’t lose weight by exercising, and because I can’t exercise, my whole body aches. I guess I will get revision surgery at the last minute, if they can still do it. The doctor told my mother that my hip might not even be able to get fixed again, so that has made me even more hesitant.”

History Of the Failed DePuy

2009

In August, the U.S. Food and Drug Administration (FDA) warns DePuy about the safety of an artificial hip device sold abroad. DePuy’s research and clinical data are inadequate, so it can’t sell the product in the United States. Meanwhile, DePuy continues to market the product outside America.

2010

DePuy begins phasing out two models of its all-metal implants that are sold in the United States. The company cites falling sales. (According to a 2012 New York Times report, DePuy actually started planning the phase-out shortly after receiving the FDA warning.) Reports of complications and high rates of early device failure have already surfaced. DePuy defends its devices by blaming failures on surgeon errors.

2010

DePuy finally recalls its Articular Surface Replacement (ASR) Acetabular Hip System and ASR Hip Resurfacing System. It cites “higher than expected revision rates” for the all-metal devices.

2011

The FDA warns DePuy to stop selling certain products, including artificial joint systems, without proper approval. It also cites ineffective quality control procedures.

2012

 DePuy Pinnacle, Another J & J Failure

  • Pain in the groin, hip or leg
  • Need for painful revision surgeries
  • Difficulty getting up, standing and walking
  • Chromium or cobalt toxicity
  • Swelling and inflammation

Metal Toxicity Symptoms

  • chest pain, shortness of breath
  • numbness, weakness, change in vision or hearing
  • fatigue, feeling cold, weight gain
  • change in urination habits
  • high levels of metal in the blood

DePuy Pinnacle, Another Failure has been recalled.

New Recall Adept Hip Replacement

Johnson and Johnson has a history of failed implants and now the Stryker Rejuvinate and ABG modular stems have been recalled.

Call our Hip Replacement Helpline today

 

 

Congress has heard the Victims of the Hip replacement Recalls

Written by lisaspitzer on . Posted in Depuy Hip Replacement News

Letter to Chairmen Upton, Pitts and Stearns, October 12, 2011

……………………………….
Congress Urge Hearing on DePuy Metal-on Metal Hip ImplantNovember 5, 2011
Congressmen Urge Hearing on DePuy Metal-On-Metal Hip Implant
 
Bloomberg Businessweek reports that a group of concerned Congressmen have written to the chairpersons of several committees, requesting hearings on the safety of Johnson & Johnson’s DePuy metal-on-metal hip implants and Boston Scientific brain stents.

The DePuy ASR metal-on-metal hip implant, which was approved under the FDA’s 510(k) approval process, in which a device can be cleared for market if it is “substantially equivalent” to devices already on the market, is known to release small metal particles into patients’ bloodstreams, potentially damaging nearby bone and tissue and necessitating painful correctional surgery. The Congressmen note that the FDA has already received over 5,000 complaints since January 2011. However, the United States does not have a registry to track medical device failure and it is possible that the number of failed devices is higher than 5,000 and will continue to rise in the coming years. The high failure rate and lack of a reliable tracking registry led the FDA “to order 20 manufactureres of these devices to submit a plan to the FDA to study how frequently they were failing and to examine the health implications of device failures.”

The Congressmen hope that hearings on the DePuy metal-on-metal hip implants will serve as a foundation to “provide important lessons about the device clearance and approval process as well as the adequacy of our postmarketing safety system.” In the past few years, Congressional “hearings on medical devices have examined claims about delays in FDA approval and overregulation,” but the letter writers believe Congress should be wary of underregulation and should examine “evidence as to whether FDA device regulation has been ineffective in protecting the public from dangerous medical devices.”

The Depuy Hip Replacement Helpline Applauds this and is waiting, watching and hopeful that dangerous drugs and medical devices get more and better regulations. Our callers are suffering and have been thru hell with revision surgeries, rehabiltiation, and a downturn in their qualityb of life. Our seniors need protection.  The FDA has failed us and we are hopeful for reform.  If you or a lovwd on has been unjured by a defective recalled hip implant call the Helpline today and speak to our medical social worker and a hip replacement recall lawyer.