Find Products Liability Attorneys That Deal With Cardiac Defribillators
Defibrillation is the definitive treatment for the life-threatening cardiac arrhythmias, ventricular fibrillation and ventricular tachycardia. Defibrillation consists of delivering a therapeutic dose of electrical energy to the affected heart with a device called a defibrillator. This depolarizes a critical mass of the heart muscle, terminates the arrhythmia, and allows normal sinus rhythm to be reestablished by the body's natural pacemaker, in the sinoatrial node of the heart.
Defibrillators can be external, transvenous, or implanted, depending on the type of device used. Some external units, known as automated external defibrillators (AEDs), automate the diagnosis of treatable rhythms, meaning that lay responders or bystanders are able to use them successfully with little, or in some cases no, training. In the event that you or your loved one was injured as a result of using one, consult a product liability attorney.
- Medtronic and St. Jude defibrillator lead defects could affect as many as 400,000 patients worldwide. If you are one of these, you should contact your doctors immediately. Have them check your records to see if your device is one of the models.
- Medtronic defibrillator leads were recalled on October 15, 2007. The Medtronic defibrillator defects include fractures of the leads, which can cause inappropriate electrical shocks and even death.
- In November 2007, it was reported in the medical literature that St. Jude Medical's Riata line of leads caused heart wall perforations in 4 patients in New York City, Nebraska and the Czech Republic. On one occasion the lead almost emerged through the skin. These perforations can lead to a fatal buildup of blood around the heart and can lead to a failure of the defibrillator to sense an abnormal heart rhythm. Both complications can prove fatal.