Personal Injury Lawyer America.com - A newsletter from the national law firm of Lieff Cabraser Heimann & Bernstein, LLP
Home button
Find a case
About Our Firm button
Contact us
SEARCH  
shim
  RECENT CASES  
   
  All Cases  
   
  GENERAL INFORMATION  
   
  Send us an email  
     
 
Safeguarding the Rights of Patients - Guidant Medical Device Failures & Defects
Introduction: Guidant Recall
Guidant Corporation, headquartered in Indianapolis, Indiana, is the second-largest manufacturer of implantable defibrillators and also manufactures pacemakers, cardiac surgery systems, and other medical devices.
Boston Scientific, which bought Guidant in 2006, announced in June 2006 the recall of more defibrillators and pacemakers. The recalled devices include Insignia and Nexus brand pacemakers, Contak Renewal TR/TR2 cardiac resynchronization pacemakers, and Ventak Prizm 2, Vitality, and Vitality 2 cardioverter defibrillators.
Position of pacemaker defibrillator in human body
Our firm, Lieff Cabraser Heimann & Bernstein, LLP, is representing Guidant patients across the U.S. in personal injury lawsuits seeking damages for the injuries they suffered due to Guidant's alleged negligence. We filed the first lawsuit in the nation against Guidant for its defective defibrillators, and are representing scores of Guidant patients with faulty heart devices.
Guidant Defibrillator Recall
Implantable defibrillator systems are used to detect and treat abnormally fast heart rhythms that could result in sudden cardiac death.
On June 17, 2005, Guidant announced a recall of nearly 50,000 heart defibrillator medical devices. Guidant expanded the recall on June 24, 2005, when the company announced an additional 46,000 devices were potentially defective. On June 26, 2006, Boston Scientific expanded the recall further.
As of October 2005, Guidant reported it was aware of over 50 reports of device failures, including three cases in which the patients died. Guidant has acknowledged that the actual rate of failure may be higher than the reported rate and that the number of associated deaths may be underreported, since implantable cardio-defibrillators are not routinely evaluated after death. To learn more about the Guidant defibrillator recall, click here.
Guidant Pacemaker Warnings
On September 22, 2005, Guidant issued a recall for some of its Insignia and Nexus implantable pacemakers because of failures, including nine cases requiring emergency hospitalization.
On July 18, 2005, Guidant alerted physicians that replacements might be needed for nine pacemaker models made between 1997 and 2000, of which some 28,000 remain implanted in patients worldwide. To learn more about the Guidant pacemaker recalls, click here.
 
Guidant heart devices
Guidant heart device defects and lawsuits
Guidant - Pacemaker Defects
Information on Guidant pacemakers, defects & lawsuits

Guidant Heart Devices Timeline
Chronological information on defects and lawsuits relating to Guidant heart devices


FDA Warning Information on Guidant Heart Devices
Warning letters and doctor and patient guidelines for Guidant devices
Our Guidant defect lawyers have years of experience successfully representing patients with faulty or defective medical implants.
There is no charge or obligation for our review of your case.
We are pleased to visit Guidant patients, or families of loved ones who died, at or near where you live and at no cost, to discuss your legal rights and answer your questions.
To assist our clients with their claims, we have on staff nurses with cardiac training and have retained physicians to provide expert advice.
Legal Rights of the Injured
The law in most states provides individuals with legal claims and the right to compensation for injuries they suffer as a result of a defective product or the negligence of another. The injured person may file a lawsuit seeking compensation for his or her pain and suffering, medical expenses, lost past and future wages and punitive damages.
Damages sought against manufacturers of an allegedly defective medical device typically include damages for:
  • Physical pain and suffering, mental anguish and physical impairment;
  • Medical expenses associated with the allegedly defective product; and
  • Loss of earnings and/or earning capacity.
About Lieff Cabraser
Founded in 1972, Lieff Cabraser Heimann & Bernstein, LLP is an over fifty attorney law firm with offices in San Francisco, New York and Nashville. For the last seven years, the National Law Journal has recognized Lieff Cabraser as one of the top 20 plaintiff law firms in America.
For our personal injury cases, we bring a team of experienced lawyers. Each client is assigned an individual lawyer. In addition, we have on staff multiple nurses, legal assistants, scientific analysts and case clerks to assist the attorneys. To learn more about our firm, click here.
     Trademark Notice: Personal Injury Lawyer America is an electronic newsletter from Lieff Cabraser Heimann & Bernstein, LLP. Lieff Cabraser represents clients in a wide range of cases, including personal injury and wrongful death lawsuits. Our personal injury attorneys | lawyers are committed to providing the very best representation and support possible for our clients.
     Lieff Cabraser is not affiliated in any way with any trademark owner. The use of any trademarks on this site is for product identification and information purposes only.
     About Lieff Cabraser: We have offices in San Francisco, New York and Nashville. Our lawyers have represented clients in personal injury, wrongful death and rollover crashes and product defect lawsuits across America.
     Disclaimer: The hiring of legal professionals is an important decision that should not be based on advertising alone. Please read our disclaimer.
Copyright © 2010 Lieff Cabraser Heimann & Bernstein, LLP

Read our Personal Injury Law brochure