|
COPYRIGHT 2005 International Medical News Group
The Food and Drug Administration has issued a nationwide notification of recall of a selection of Guidant implantable defibrillators and cardiac resynchronization therapy defibrillators.
The models affected are the Prizm 2 DR Model 1861 implantable cardioverter defibrillators (ICDs), manufactured on or before April 16, 2002, and two cardiac resynchronization therapy defibrillator (CRT-D) models, the Contak Renewal, model H135, manufactured on or before Aug. 26, 2004, and the Contak Renewal 2,...
Read the full article for free courtesy of your local library.
|
Bookmark this article
Print this article
Link to this article
Email this article
Digg It!
Add to del.icio.us
RSS
