Personal Injury for Accidents, Injuries, Defective Products, Drug Liability, Slips & Falls, Dog Bites, Malpractice
|
|
|
Guidant Defibrillator Recall
The FDA is notifying health care providers and patients that the Guidant Corporation is recalling certain of its implantable defibrillators and cardiac resynchronization therapy defibrillators. These devices can develop an internal short circuit without warning, resulting in failure to deliver a shock when needed. The devices affected by this notification are:
"FDA's first priority is patient safety," said Daniel Schultz, MD, Director of FDA's Center for Devices and Radiological Health. "We want to ensure that all patients who may be affected by this problem are notified and seek appropriate medical advice from their physicians." FDA is not making a recommendation on whether individual patients who have one of the Guidant devices should have it removed and replaced. This is a decision that should be made by a patient in consultation with his or her physician, based on the specific medical situation of the patient. Removal and replacement of the device may pose some risk, so it is important that patients and physicians carefully discuss this matter before making a decision. FDA advises patients to take the following steps:
See your doctor if you have received a Guidant defibrillator device and you are concerned about your safety. If you or a family member has been injured, abused or otherwise harmed, you should contact one of our California attorneys who can help you protect your legal rights. Please keep in mind that there may be time limits within which you must commence suit. You may also contact us by calling toll-free: 1-800-616-4529 Return to Top of Page |
|
Free Consultations, Certified Attoneys, Cases taken on Contingency Including Accidental and Wrongful Deaths.
|
|
|
|