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: Charlotte Personal Injury LawyerRecall of certain Medtronic Kappa and Sigma Series pacemakers
By Greg Jones
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.
Originally posted at InjuryBoard by Greg JonesFull post as published by Charlotte Personal Injury Lawyer on June 11, 2009 (boomark / email).
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