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 ...

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.

The FDA first approved home models of Philips AED devices in 2004. The defibrillators under question were manufactured and distributed between 2005 and 2012 under the names HeartStart FRx ...

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 ...

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 ...

For example, pay attention to the following HeartStart Home Defibrillator from Philips. To put it short, this HeartStart Home Defibrillator is among the safety equipment that you can use to ...

The FDA has approved Royal Philips' (NYSE:PHG) premarket approval applications (PMAs) for its HeartStart FR3 and HeartStart FRx automated external defibrillators (AEDs) and supporting accessories.

Philips’ HeartStart OnSite and HeartStart Home defibrillators are the only over-the-counter automated external defibrillators (AEDs) available to consumers in the US, while the HeartStart Home ...

The therapy delivered by the HeartStart FR2+ is the most proven in the industry. More than 40 studies confirm its effectiveness. Philips’ high-current/low energy therapy ensures a potent ...

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 ...