Philips Recalling 5,400 FR2+ Automated External Defibrillators
Philips is recalling some 5,400 defibrillators from their professional line, the FR2+ due to a problem with a memory chip that is experiencing a high rate of failure and will lead to the defibrillator unit being inoperable. The units detected the problems during the self-test routines and not during acutal emergency usage.
The defibrillator recall affects models M3860A and M3861A distributed by Philips as well as models M3840A and M3841A distributed by Laerdal Medical. All the recalled defibrillators were manufactured between May 2007 and Janry 2008.
See Philips Recall Information
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