Medtronic lead recall 6949 Sprint Fidelis lawsuitOn October 15, 2007, Medtronic informed patients with Sprint Fidelis lead Model 6949 that their defibrillation lead was recalledhe Medtronic recall also affected patients with lead Models 6930, 6931 and 6948atients can identify which Medtronic lead they have by referring to their Patient ID card (wallet card) which will contain the model of their implanted leadf a patient is unsure about which lead they have implanted they should consult with their physician total of 268,000 Sprint Fidelis leads were implanted worldwide, with 172,000 leads implanted in the United Statess of January 2007, approximately 144,311 Medtronic Sprint Fidelis Model 6949 leads had been implantedmplantable cardioverter defibrillators (ICDs) and Cardiac Resynchronization Therapy-Defibrillators (CRT-Ds) are used to treat abnormal heart rhythms in patients which can cause the heart to suddenly stopCDs and CRT-Ds shock the heart back into typical rhy ... [Read More - Forex Signals App]
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