Pacemaker Recall

[cmooredavis]

Medtronic Issues Pacemaker Recall

They include devices in the Kappa Series 600/700/900 and Sigma Series 100/200/300 manufactured primarily between November 2000 and November 2002.

http://www.medpagetoday.com/ProductAlert/DevicesandVaccines/14677?userid=157659&impressionId=1245033922089&utm_source=mSpoke&utm_medium=email&utm_campaign=DailyHeadlines&utm_content=Group1