Patients with a myocardial infarction are at an increased risk of sudden cardiac death largely due to ventricular arrhythmias associated with myocardial scarring. Implantable cardioverter defibrillators (ICDs) have been established as the best available treatment for the secondary prevention of an arrhythmic death in patients at high risk. This includes patients who have survived sudden cardiac death, have had sustained ventricular tachycardia or fibrillation, or have had syncope assumed to be due to a ventricular arrhythmia. High-risk features of patients with infarction without a previous arrhythmic event who qualify for a primary prevention ICD are an ejection fraction (EF) <30% or symptoms of Class II or III heart failure with an EF≤35%. In addition, patients with nonsustained ventricular tachycardia, a positive electrophysiology study, and EF≤40% are candidates under the current primary prevention guidelines. The current guidelines have specified the timing for ICD implantation as >40 days following the acute myocardial infarction. Despite the establishment of the guidelines, current clinical practice has revealed that ICDs are underutilized in patients who qualify. This article reviews the ICD implantation guidelines to encourage the appropriate use of the device.