Medtronic Sprint Fidelis

After deaths of five patience that have been linked to the devices, Medtronic Inc. has removed its Sprint Fidelis defibrillation leads from the market. A fracture in the defibrillator lead can cause a defibrillator to deliver unnecessary shocks to the heart or not operate at all. These defibrillators are used to regulate a persons heartbeat. If you or a loved one or someone you know has a debibrillator implanted that uses a recalled Medtronic Sprint Fidelis lead, you may have valuable rights. The defibrillators that are at risk are Sprint Fidelis 6930, Sprint Fidelis 6931, Sprint Fidelis 6948, and Sprint Fidelis 6949. Mark & Associates, P.C represents all defective medical device clients. There will be no legal fees unless they win your case. You can call them toll free or give them information online.