6/13 Food and Drug Adminstration (FDA): CDRHNew

Please add updates@feedmyinbox.com to your address book to make sure you receive these messages in the future. Food and Drug Adminstration (FDA): CDRHNew Class I Medical Device Recall: Medtronic Inc., Kappa 600/700/900 Series of Pacemakers and Sigma 100/200/300 Series of Pacemakers June 12, 2009 at 12:00 am Reason for Recall: The Kappa and Sigma pacemakers in these identified series may fail due to a separation of wires that connect the electronic circuit to other pacemaker components, such as the battery.   This email was sent to skripayura.drugsnews@blogger.com.  Create Your Account Don't want to receive this feed any longer? Unsubscribe here.