Guidant Defibrillator Recall Information
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Guidant Recall Alert!
On Wednesday, December 14, 2005, the FDA announced that it has received reports of recent patient deaths linked to fatal complications in heart devices manufactured by Guidant Corporation.

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Contact Information
Fill out the following form or call 1-866-722-8700 24 hours a day, 7 days a week for a Free Case Review.
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Injured Person's Contact Information
The injured person is
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Did you or your loved one have a Guidant Defibrillator implanted?
YesNo
If yes, what type of Guidant defibrillator was it?
Did you or your loved one have a Guidant Pacemaker implanted?
YesNo
If yes, what type of Guidant pacemaker was it?
When was the defibrillator/pacemaker implanted?
Why was the defibrillator/pacemaker implanted?
Has the defibrillator/pacemaker malfunctioned?YesNo
Were you or your loved one injured as a result of the malfunction?YesNo
Do you or your loved one currently have an attorney helping you with your potential Guidant recall case?YesNo
Additional Comments or Questions:
a. I agree that submitting this form and the information contained within does not establish an attorney client relationship.
b. I agree that my information will be reviewed by more than one attorney and/or law firm.
c. I agree that the information that I will receive in response to the above question is general information and I will not be charged for the response to this e-mail question. I further understand that the law for each state may vary, and therefore, I will not rely upon this information as legal advice. Since this matter may require advice regarding my home state, I agree that local counsel may be contacted for referral of this matter.