An Automated External Defibrillator (AED) is a device used when someone is experiencing certain types of cardiac arrest. In cardiac arrest, or sudden cardiac death, the heart’s electrical activity is disorganized and there is no effective pumping of blood. An AED is capable of recognizing the heart's electrical activity, determining if an electric shock is required, and restoring normal heart rhythm.
AED devices are safe. They are programmed to deliver shocks only when the heart rhythm is not effective and the electric shock is definitely required. If the shock is needed, a voice prompt in the AED is activated, telling the rescuer to push a button to deliver the shock. The device is only applied when a person has collapsed in cardiac arrest, has no effective breathing or coughing, and no movement. An AED should not deliver an electric shock if applied by mistake to a person who has fainted or had a seizure.
California law allows the placement and use of AEDs in the home, work settings, and other public locations. Rules for training vary depending on whether the AED is for a specific individual, or for use in a public setting. Orange County Emergency Medical Services should be notified when an AED device is located in a private or public setting anywhere in the County of Orange. Specific information related to AED program requirements can be found by viewing the California Code of Regulations, Title 22, Ch. 1.8 and other provided in links on this page.
PHILIPS Healthcare - HeartStart Operations Product Name: HeartStart Defibrillators Sales Contact: Bryan Flynn (877) 443-2994 34145 Pacific Coast Highway #101, Dana Point, CA 92629
Ray of Life Product Name: Any and all AEDs available for purchase Helena Jacobson 949-768-7447 25422 Trabuco Rd #105-477 Lake Forest, CA 92630
Zoll Medical Corporation Product Name: Zoll AED Sales Contact: Catherine Prophet 800-242-9150, ext. 571 32 Second Avenue Burlington, Mass 01803-4420
For more information
Contact Orange County Emergency Medical Services, 714-834-3500.
Class I Recall of certain LIFEPAK CR Plus Automated External Defibrillators (AED) mfg and distributed from July 9, 2008 through August 19, 2008. Read More
Class I Recall has recently been updated Recalls for U.S. Food & Drug Administration (FDA). Information about the Physio Control, Inc. LifePak CR Plus Automated External Defibrillators (AEDs) Class I Recall has recently been updated, and is now available. Read More
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