FDA Alerts Patients to Medtronic Pacemaker Recall

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Title: FDA Alerts Patients to Medtronic Pacemaker Recall

FDA Alerts Patients to Medtronic Pacemaker Recall
Thu, 11 Jun 2009 13:04:00 -0500

The U.S. Food and Drug Administration is alerting patients to the Class I recall of certain Medtronic Kappa and Sigma pacemakers. These devices may fail due to a separation of wires that connect the electronic circuit to other pacemaker components, such as the battery.


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