Alert – Don’t Be The Next Victim

Humankind No.1 killer disease, cardiovascular disease (CVD) always dominate the top disease killer ranking all around the world. According to the American Heart Association's Heart Disease and Stroke Statistics, although this main killer death rate have experience some declining since the last few year, but is still remain the No.1 cause of death in the United States last year.

Those diseases that categorized in the cardiovascular disease (CVD) are:

  • heart disease,
  • heart failure or disorder,
  • high blood pressure,
  • stroke,
  • atrial fibrillation,
  • arrhythmias,
  • cardiomyopathy and
  • peripheral arterial.

A partial of the heart diseases related patient that suffered from the seriously hearth dysfunctional, need to survive with the Sprint Fidelis Defibrillator Leads. What is this Defibrillator leads? This Sprint Fidelis Leads is the product by U.S.A. well-known Medtronic Inc; it is a specific model of cardiac electrodes, where it’s connected an implantable cardioverter-defibrillator (ICD) directly to the heart.

The Medtronic Inc started to remove all of the Defective Defibrillator Leads after five patients that used this product encounter death that been discovered by the irregular shocks to the patient’s hearth. This company has begun to ask all U.S.A. doctors to stop using this lead to the patient and return all of the unused lead to Medtronic as soon as possible.

A Defibrillator Lead Recall has implemented to take backs all of the fracture or may be in risk leads such as:

• Sprint Fidelis 6930
• Sprint Fidelis 6931
• Sprint Fidelis 6948
• Sprint Fidelis 6949

For those that been injured during the period of using this lead, they may be qualified to receive a sum of compensation from those that responsible for this injury causing.

Be cautious about this kind of Defective Defibrillator Leads; it is not only will help to prolong your life span but also will be a fatal killer as well!

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