Medtronic Pacemakers Recalled
Medtronic pacemakers are recalled on 05/18/2009 by the FDA.
This is a Class 1 recall, the most serious type of recall action. The major concern of the recall was its failure, “due to a separation of wires that connect the electronic circuit to other pacemaker components, such as the battery.” The malfunctioning pacemakers can cause abnormal heart rates, fainting or lightheadedness. More serious concerns are serious injury or death.
The affected pacemakers are Kappa Series 600/700/900 and Sigma Series 100/200/300 manufactured primarily between November 2000 and November 2002. Most were implanted at least 5 years ago.
The Pintas Law Firm is currently investigating these claims. If your pacemaker is affected by this recall contact our firm now for additional free information. See the following websites for more information on the recalled pacemakers and the adverse health effects they may cause:
wwwp.medtronic.com/ProductLookup/lookup.html
wcms.fda.gov/ucm/groups/fdagov-public/documents/image/ucm162880.gif
