Philips Issues Worldwide Recall of Select Heartstart Fr2+ Automated External Defibrillators
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Philips Issues Worldwide Recall of Select Heartstart Fr2+ Automated External Defibrillators
fda.gov —
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.
View full resource at fda.gov
Tags: Advanced Life Support, Memory
Most Recently Shared on October 4, 2009 at 12:41 pm By:
Recall: 5,400 HeartStart FR2+ automated external defibrillators (AEDs) with bad memory chips: http://tinyurl.com/yevnons
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