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Guidant Lawsuits:
Guidant Defibrillator Recall Lawsuits
Guidant Defibrillator Recall Lawsuits
Guidant Defibrillator Recall Lawsuits
Guidant Defibrillator Recall Lawsuits
 

Guidant Defibrillator Recall

Do I have a Guidant defibrillator recall lawsuit?

What are the defects involved in Guidant defibrillator recall lawsuits?

What is the problem with the Guidant defibrillator?

Who is responsible for the Guidant defibrilattor recall lawsuits?

What is being done - Guidant defibrillator recall lawsuits?

What can you do about the Guidant recall?

Do I have a Guidant defibrillator recall lawsuit?

Guidant defibrillator recall FAQs

 

 

Guidant Defibrillator Recall Lawsuits

While you may have a Guidant defibrillator implant to save your life, a defect in the product could cost you your life. Learn more about which models have a flaw and whether your model may qualify you for a defibrillator replacement the steps being taken by Guidant lawyers on behalf of the defendants and plaintiffs, and whether you should file a Guidant defibrillator recall lawsuit. There are many models of Guidant Defibrillators that are the subject of a recall by the company.

Over the course of weeks during June and July, 2005, the company, Guidant, has added a number of additional models. There are now as many as 20 models that have been the subject of a recall and/or a warning. Thus, even if you originally thought your model was not covered by the recall, you should check again to see if your model has been added to the list of Guidant defibrillators that have now been recalled. Guidant lawyers are familiar with which models are at risk.

If you have a Guidant defibrillator, you should check with your doctor to see if it has been recalled. Many patients have called their doctors after the announcement on June 20, 2005 that Guidant has sold faulty implanted heart defibrillator devices. In addition, you should be aware that originally Guidant advised that some defibrillator models could re-programmed, but has since changed its warning on these models as well, and urges replacement of many of these. Replacement is something you should discuss with your doctor.

As of June 20, 2005, Guidant had offered to replace thousands of these defibrillator devices due to flaws that have been found in as many as 20 models. Additional units have been added to the list of recalled defibrillators, and thus you should re-check to see if your model was added. Guidant has an online tool that you can use to see if your serial number is one that is subject to the recall. Or you can contact a Guidant lawyer to see if your model is part of the recall.

Ask a Guidant lawyer about Guidant lawsuits: Do you have a Guidant Defibrillator recall lawsuit?
Do you, a family member, or dear friend use a Guidant Defibrillator? Are you concerned about the device failing as a result of flaws? You may have a Guidant defibrillator recall lawsuit and could be included in the nationwide Guidant class action or mass action lawsuit. To consult with a lawyer familiar with Guidant defibrillator recall lawsuits, please complete our FREE no obligation consultation form today.
 



 


Ask a Lawyer: Do I have a Guidant Defibrillator Recall Lawsuit?

Do I have a Guidant Defibrillator Recall Lawsuit? You may need a lawyer to represent you. Learn more by filling out the form below! Lawyers and experts ready to help you now.

Guidant Defibrillator - Lawyers ready to Help.
Free Consultation form below for the Monheit Lawfirm.

First Name:
Last Name:
E-mail Address:
Phone: () - ext.
Address:
City:
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Age:
Date of Birth:

What complications have you had from the Guidant defibrillator implant?
For What recommendations have your doctors made about removing this device?
For Please list any relevant Surgeons, Hospitals, and Cardiologists who are treating or have treated you with respect to the Guidant implant. (Please include city & state)
Implant Date: What was the date you received your implant?
If removed, what was the date of REMOVAL of your implant?
Which manufacturer's device has been implanted? (please check all that apply)
GUIDANT
MEDTRONIC defibrillators
Which device(s) have been implanted? (see ID Card for Model #) (please check all that apply)
Ventak Prizm 2 DR (Model 1861), prior to April 16, 2002
Contak Renewal (Model H135), prior to Aug. 26, 2004
Contak Renewal 2 (Model H155), prior to Aug. 26, 2004
Ventak Prizm AVT
Vitality AVT
Renewal 3 AVT
Renewal 4 AVT
Medtronic Concerto
Unknown or Other
Additional Guidant Recall Lawsuit Information: Please be specific and tell us about your experience with the Guidant Defibrillator. Also enter any questions or comments in this space.


 
Guidant Defibrillator Recall Lawsuits
 
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