The FDA has issued a preliminary analysis of the Cardiac Science Powerheart and CardioVive
Automated External Defibrillator(AED) G3 Series manufactured between
August 2003 and August 2009. Affected models include the following:
Powerheart models 9300A, 9300C, 9300D, 9300E, 9300P, 9390A, 9390E; and
CardioVive 92531, 92532 , and 92533
Problem and…
Read More