Philips recalled three models of its HeartStart devices in September 2012 due to an internal electrical malfunction. The recall affects about 700,000 defibrillators sold between 2005 and 2012.

If you still own one of these devices, contact Philips Healthcare for a replacement AED unit. In North America, you can call 1-800-263-3342 or email [email protected].

SEATTLE -- Philips said Monday it is recalling about 5,400 HeartStart FR2 automated external defibrillators due to a possible memory chip failure that could make the device unable to work properly.

May 2, 2005 — The U.S. Food and Drug Administration (FDA) and Laerdal Medical Corp. have notified healthcare professionals via letter of a recall of all lots of CM 100-Heartstart defibrillator ...

Philips recalled its HeartStart MRx Defibrillator due to an equipment defect, according to a Feb. 9 safety notice from the FDA. Here are three things to know. 1. Philips initiated the recall in ...

In case your fibrillator need defibrillating, Philips is poised to bring this automatic defibrillator to market once the FDA approves direct-to-consumer sales of the devices. You've seen these on ...

The Philips HeartStart OnSite Defibrillator is designed to be the easiest-to-use, and most reliable defibrillator available. Available without a prescription from ActiveForever.com, the Philips ...

Help Save a Life with Philips HeartStart Home Defibrillator. 2011-11-25T11:25:56Z ... this HeartStart Home Defibrillator is among the safety equipment that you can use to protect yourself and your ...

We know what you're thinking: not another talking defibrillator, but the Q-CPR add-on to Philips' HeartStart MRx monitor/defibrillator actually happens to be the first of its kind, and was ...