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Greg Jones
Greg Jones
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Recall of certain Medtronic Kappa and Sigma Series pacemakers

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The FDA just announced Class I recall of certain Kappa and Sigma Series pacemakers, because these devices may fail due to a separation of wires that connect the electronic circuit to other pacemaker components. Medtronic Kappa Series 600/700 and 900 as well as Sigma Series Series 100,200 and 300 pacemakers were involved in the recall.