Philips Issues Worldwide Recall of Select Heartstart Fr2+ Automa...

Courtesy Food and Drug Administration--Recalls  Sat, 10/03/2009 - 06:30

Philips announced today that it is voluntarily recalling approximately 5,400 HeartStart FR2+ automated external defibrillators (AEDs).

This recall is being conducted due to the possibility of a memory chip failure that may render the device inoperable.

Only certain HeartStart FR2+ AEDs (models M3860A and M3861A, distributed by Philips; and models M3840A and M3841A, distributed by Laerdal Medical) manufactured between May, 2007 and January, 2008 are included in the voluntary recall.

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