Some defibrillation leads made by Medtronic are being recalled because they have been linked to patient deaths. The defibrillation lead, when fractured will give unnecessary shocks to the heart or not operating at all. Doctors have been requested to stop implanting them on patients. Users of the Medtronic Sprint Fidelis 6930, Sprint Fidelis 6931, Sprint Fidelis 6948, & the Sprint Fidelis 6949 are advised to seek free consultation from the defective medical device attorneys as soon as possible. Folks who are unsure whether their defibrillators are among the ones being recalled should also request a free evaluation from Mark & Associates, P.C. They will be represented on a contingency basis & only pay legal fees for a winning compensation.
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