Kahn Gauthier Swick is seeking to file a lawsuit on behalf of persons that have certain Medtronic implantable heart devices. These products were surgically implanted in persons that are either prone to life-threatening heart rhythms, congestive heart failure or a combination of both.
However, on February 11, 2005 Medtronic Inc. issued a statement that the company was voluntarily advising physicians about a potential battery shorting mechanism in certain implantable cardioverter-defibrillator (ICD) and cardiac resynchronization therapy defibrillators (CRT-D) models. This could cause the battery to experience a rapid depletion of power resulting in the loss of device function. This would prevent the device from correcting the abnormal heart rhythm. If you or a loved one believe you have one of these heart devices please contact the Kahn Gauthier Swick for more Medtronic lawsuit information.
ICDs shock the heart back into a regular rhythm if the patient suffers a life threatening arrhythmia that could lead to cardiac arrest. CRT-Ds provide electrical impulses to improve heart function.
The particular ICDs and CRT-Ds were manufactured between April 2001 and December 2003 and include the following:
Model 7230 Marquis™ VR
Model 7274 Marquis™ DR
Model 7232 Maximo™ VR
Model 7278 Maximo™ DR
Model 7277 InSync Marquis™
Model 7289 InSync II Marguis™
Model 7279 InSync III Marquis™
Model 7285 InSync IIIProtect™ (No devices implanted in the U.S.)
These are the only models that are affected. Please contact Kahn Gauthier today by either calling us at 1-866-467-1400 or clicking on this page to make a claim if you believe that you have one these ICDs or CRT-Ds or if your physician has contacted you regarding having your ICD or CRT-D replaced.