Philips Issues Worldwide Recall of Select HeartStart FR2+ AEDs

Apr 13, 2010

On September 28, 2009, Philips announced a worldwide recall on the HeartStart FR2+ AEDS. The recall is a voluntary recall, it was not mandated by the FDA. Philips is recalling the HeartStart FR2+ AEDs that were manufactured during May, 2007 thru Janurary, 2008.


The reason for the recall is due to a faulty memory chip in the Philips HeartStart FR2+ AED. Philips is concerned that the memory chip may fail and cause the AED not to function properly.


If you are concerned that your Philips HeartStart FR2+ AED may be part of the recall, you can click on the link below and check your serial number. If you have any questions in regards to the recall or your HeartStart AED, you can contact Philips at 1-800-263-3342.


www.philips.com/FR2PlusAction

If you are interested in the full story that this blog was based on, please click here.

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