Company warns of heart device malfunctions

Implanted heart device manufacturer Medtronic of Minneapolis is asking doctors to discontinue use of a component in its newest defibrillator models.

Medtronic said the component, an electrical wire that connects the defibrillator to a patient's heart, is prone to defect and has been linked to hundreds of malfunctions and may have been involved in five fatalities, The New York Times reported Monday.

The company also urged the approximately 235,000 patients who have been outfitted with the devices to have them immediately examined by doctors to ensure they are properly reading heart rhythm data.

The move was welcomed by Daniel Schultz, director of the Center for Devices and Radiological Health at the U.S. Food and Drug Administration.

"Medtronic's decision to voluntarily remove its Sprint Fidelis defibrillation leads from the market is in the best interest of patient safety," Schultz said in a statement.

"These electronic wires are prone to fracture in a small number of patients which can cause the defibrillator to deliver unnecessary shocks or not operate at all. Based on our initial review of reported adverse events, some deaths and major complications have occurred after the leads have fractured," he said.

Copyright 2007 by United Press International


Explore further

Rate of heart complications low for Aussie COVID-19 patients

Citation: Company warns of heart device malfunctions (2007, October 15) retrieved 26 September 2021 from https://medicalxpress.com/news/2007-10-company-heart-device-malfunctions.html
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only.
 shares

Feedback to editors