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We are currently investigating cases involving the failure of Guidant Corporation defibrillators and pacemakers.
Manufacturers of medical devices such as defibrillators and pacemakers have a duty to be sure those devices are free from defects and work as intended.
Since June of 2005, Guidant has recalled thousands of its implantable cardiac medical devices. There are approximately 50,000 patients in the United States with one of these recalled medical devices called defibrillators. These devices have been known to malfunction resulting in an inability to deliver the required shock during episodes of arrhythmia.
These medical device failures have required the removal and replacement of the recalled models, which if left unattended, could cause injury or death should the device fail. A separate surgery may be required to replace these defective medical devices.
Whether your injuries were caused by a defect in product design, production or quality control problems, you have the right to seek compensation, call us now at 1-800-416-8010.
Whatever the reason when you've been in an accident, you need help NOW. If you or a family member have suffered as a
result of a defective medical device, call us now at 1-800-416-8010 or simply submit a short and simple case evaluation form. Help is just a "click" or "call" away and we'll get started on your case today — "It's Just That Easy".
CLICK HERE TO START YOUR CASE
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