Medtronic Defribillators

Medtronic defibrillators have been identified as defective medical devices. If you have been injured by an implantable defibrillator like a Guidant defibrillator, you should contact an attorney.

Medtronic Defribillator Identified as Defective and Recalled

Treating heart disease and problems, specifically dangerous heart rhythms with technology has become commonplace. Both pacemakers and implantable cardioverter defibrillators are used in patients to combat dangerous heart rhythms like ventricular tachycardia or fibrillation.
 
In the case of implantable defibrillators, when the unit detects a dangerous heart rhythm, it sends a small shock to the heart to restore a natural and healthy rhythm. These devices are implanted beneath the skin in the chest or abdominal cavity and are smaller than a wallet in size. There are small leads going from the unit to the surface or interior of the heart and this is how the electric shock moves from the unit to the heart itself. The units typically have additional functions, including the ability to maintain data about a patient’s heart rhythms for doctors to study and the ability to conduct non-invasive testing on a patient’s heart throughout the course of treatment.
 
As is the case with most medical devices, some internal defibrillators have failed to work as prescribed and caused some health problems. For instance in February of 2005, Medtronic issued a recall on over 80,000 of its implantable defibrillators, citing a battery problem that might inhibit the ability of the unit to properly monitor and treat dangerous heart rhythms. The Medtronic defibrillators that were affected by this battery malfunction were made between April of 2001 and December of 2003.
 
These Medtronic defibrillators included the Marquis VR 7230, Marquis DR 7274, Maximo VR 7232 and the Maximo DR 7278. There was also an issue with their cardiac resynchronization therapy defibrillators including the InSync I Marquis, InSync II Marquis, InSync III Marquis, InSync III Protect 7277 and the InSync III Protect 7289.
 
Despite the recall issued, Medtronic is still liable for any damage or illness caused by the failure of their defibrillators. In this case, it appears that a design flaw has contributed to their product liability, but an experienced attorney is the only one who can truly advise you on whether or not you have a claim.
 
If you, or someone in your family has one of these defective Medtronic defibrillators, you may have the opportunity to have it replaced free of charge and for a complete reimbursement of any medical fees for the original implant. If you have lost a family member or you have been hurt or incapacitated due to the failure of a Medtronic defibrillator, you may be entitled to compensation for pain and suffering and loss of income.
 
No matter which position you are in, you should contact a reputable and experienced product liability or medical device defect attorney. They will know whether you have a case and if you do, how best to file. While some cases may be strictly based on product liability and medical device malfunction, others may have a case relating to medical malpractice. There are also several class action lawsuits pending that are related to internal defibrillators. Speak to an experienced attorney as soon as possible to assess your case and to ensure that you don’t miss your opportunity because of statute of limitations.

 

Informative Articles About Medtronic Defibrillators

· The Medtronic Recall: A Breach of Public Trust in Defective Medical Devices

  4/10/2006 4:45:00 PM | Medtronic's Defibrillator & Pacemaker Recall

 Latest Medtronic Defibrillators & Related Newswire

· Medtronic Lawsuit Filed Over Defibrillator Battery Defect - Madison County Record

  6/12/2006 4:23:00 PM | Medtronics targeted in St. Clair County again
  Comments:(0)
   Medtronic is being sued by an Illinois man, claiming damages because the implantable defibrillator he received was later revealed to have a defective battery. He was subsequently hospitalized and is claiming personal and economic damages. The 24 counts in the lawsuit include fraud, negligence, misrepresentation and defective design.
     Read More

· Medtronic Adopts Doctors' Society Guidelines - MarketWatch

  5/15/2006 12:51:00 PM | Medtronic outlines its initiatives on pacemaker guides
  Comments:(0)
   Medtronic, a medical device maker, has outlined improvements it is implementing to adhere to the guidelines recently recommended by the Heart Rhythm Society: It is expanding its panels that study performance trends and quality control; it is creating a patient advisory panel to improve communication with patients; it will work to pool data fro...
     Read More

· New Implantable Defibrillator Studied - Twin Cities Business Journal

  5/10/2006 11:01:00 AM | Medtronic begins study on new ICD device
  Comments:(0)
   Medtronic has begun a clinical trial to study a new device in the treatment of mild to moderate heart failure. The device is an implantable defibrillator, but also is able to transmit data via phone lines so that doctors can more closely monitor patient heart rate, pressure, body temperature and activity.
     Read More

· Minnesota Woman Works to To Improve Medical Device Defect Recall Communication - Mankato Free Press

  3/19/2006 12:20:00 AM | Heart of the matter
  Comments:(0)
   Susan Peterson, a Minnesota woman who was implanted with a Medtronic heart medical device to help her enlarged heart condition, found it difficult to get facts from Medtronic when they issued a recall for her medical device. Once the truth came to light, her Medtronic defibrillator was immediately replaced and she now works to secure improved legislation for medical device patients so they can get the information they need to make informed decisions.
     Read More

· Medtronic Wins FDA Approval for Expanded Pacemaker Labeling - Twin Cities Business Journal

  3/17/2006 9:40:00 AM | Medtronic expands pacemaker labeling
  Comments:(0)
   Medtronic, Inc. makers of medical devices like pacemakers and defibrillators has received FDA approval to expand the use of their pacemakers. The approved new labeling of the devices will allow doctors to prescribe them to a larger group of patients. No details were released as to the new applications of the Medtronic pacemakers. Medtronic has been...
     Read More


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Defective medical devices seem to be released more often as our technology increases. With so many innovations, sometimes the oversights can be as small as a defective battery that causes a pacemaker to malfunction. If you feel you have been harmed by a Boston Scientific Stent, Medtronic Defibrilator or other medical product, simply fill out the form below and we'll pass your information to a Lawyer that can give you more informaiton.

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