Guidant Device Recall

MEDTRONIC RECALL
Defibrillator Replacement

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Medtronic Defibrillator Lawsuits
Recall cases handled by Monheit Lawfirm

 

What does Medtronic do?
Medtronic is a medical device company. They manufacturer a number of implantable medical devices, including medtronic heart defibrillator (Medtronic Insync cardiac resynchronization therapy defibrillator, Maximo ICD and Marquis ICD models). Medtronic is headquartered in Minneapolis, Minnesota.

What is the problem with the Medtronic defibrillator?
In February 2005 Medtronic notified the FDA, doctors and patients, that a number of its implantable defibrillator (Medtronic Insync cardiac resynchronization therapy defibrillator, Maximo ICD and Marquis ICD models) fail suddenly, because they have a defective battery. Device failure can result in sudden death. The devices with a bad battery were put into services as Medtronic ICD devices in 2001, 2002, and 2003.

Medtronic announced that two specific types of ICD devices (implantable cardioverter defibrillator) may suffer from a leaking battery charge (a bad medtronic battery that result in power depletion) that causes the device to suddenly fail without warning. There are two types of Medtronic heart devices subject to this recall. These are: cardioverter- defibrillator (ICDs) and cardiac resynchronization therapy defibrillator (CRT-D) devices.

What models are defective?
Implantable cardioverter-defibrillator models: Marquis VR 7230, Marquis DR 7274, Maximo VR 7232, and Maximo DR 7278.

What about Medtronic Cardiac resynchronization therapy defibrillator?
InSync Marquis 7277, InSync II Marquis 7289, InSync III Marquis 7279, and InSync III Protect 7285.

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

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What complications have you had from the Medtronic 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 Medtronic 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 device(s) have been implanted? (see ID Card for Model #)
(please check all that apply)

   Model 7230 Marquis VR

   Model 7274 Marquis DR

   Model 7232 Maximo VR

   Model 7278 Maximo DR

   Model 7277 InSync Marquis

   Model_7289_InSync_II_Marquis

   Model 7279 InSync III Marquis

   Model 7285 InSync III Protect

   Unknown or Other

Additional Information:
Please be specific and tell us about your experience with the Medtronic Defibrillator. Also enter any questions or comments in this space.


 

 

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