MedPage Today -- The FDA announced a voluntary recall of certain models of the HeartStart FR2+ brand of automated external defibrillator (AED) because of a memory chip failure, which can render the device inoperable.
MedPage Today -- The FDA announced a voluntary recall of certain models of the HeartStart FR2+ brand of automated external defibrillator (AED) because of a memory chip failure, which can render the device inoperable.