Philips Voluntary Recall; AED, Automated External Defibrillator, Defibrillator

Jun 2, 2010

Philips has announced a voluntary recall on the Philips HeartStart OnSite and the Philips HeartStart FRx automated external defibrillators (AEDs).

The Philips voluntary recall that has been issued is for a small amount of affected Philips OnSites and Philips FRx AEDs. The reason for this voluntary recall is due to the fact that a relay in the devices is not up to Philips' performance standards. The affected relays came from one manufacture and were in a single lot. There have been no reports of the device's relay failing, but the potential of failure does not meet Philips' standards.

The Philips AEDs that were affected by the recall were manufactured during March 2010. Philips is contacting the customers directly in regards to this matter.

If you have not been contacted and you are concerned that your AED may be part of the recall, you can input your serial number and it will search their system to verify that your AED is or is not on the recall list. Click here to input your serial number.

It read more about the recall, please CLICK HERE.

Contact HeartSafe America if you have any questions regarding your AED, AED replacement accessories, or general questions about AEDs and Sudden Cardiac Arrest. Our goal is to educate the public about Sudden Cardiac Arrest and how AEDs can increase the survival rate.

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