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Ischaemic Myocardium Defibrillators: Have You Been Hurt?
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BREAKING NEWS: 10.15.07--Medtronic, Inc., the world's largest maker of electronic heart devices, announced they are suspending sales of Sprint Fidelis leads. According to the FDA, these wires, used to connect defibrillators to the heart, may break or erode and may increase chance of injury. Learn more about the Medtronic Sprint Fidelis Recall. |
Did your Ischaemic Myocardium Defibrillator harm
you? Did you trust it to save your life and have it almost take it instead?
Know that you are not alone. The FDA has recalled several malfunctioning models
of this potentially dangerous device.
Myocardial
ischaemia is generally defined as a physical malady in which the heart
doesn't work properly, and blood cells are injured. In this situation,
myocardial ischaemia can manifest itself in several different ways:
If you have been injured by this harmful device, contact the legal experts, and receive a free case review.
If your or a loved has
had an implantable cardioverter-defibrillator such as the recalled Guidant:
1. CONTAK RENEWAL 2,
Model H155
2. CONTAK RENEWAL, Model
H135, or
3. PRIZM 2 DR, Model 1861
An experienced attorney
can help protect you!!!
Defibrillators were
designed to save life, not put it at a greater risk. Fill out the simple
form below to contact an experienced defibrillator lawyer before your time limit
to file suit runs out.
Weitz & Luxenberg is no longer accepting Guidant Defibrillator cases.
see also:
Arrhythmias
Arrhythmias: Guidant Lawsuit Information, FREEArrhythmias, FREE Guidant Defibrillator Lawsuit info
Phosphate Compounds
High energy phosphate compounds: Guidant Lawsuit Information, FREEHigh energy phosphate compounds, FREE Guidant Defibrillator Lawsuit info
Electrophysiology
Find out more about the Electrophysiology of Guidant Defibrillators Electrophysiology of Guidant Defibrillators
