LIFEPAK 20 and LIFEPAK 20e External Defibrillator/Monitors by Physio-Control Inc. - Class I Recall
MedSun: Newsletter #51, August 2010

FDA MedWatch Safety Alert

Failure on the power supply assembly can result in either "No DC power" or "No DC or AC power". A failure of DC (battery) power can result in the inability to deliver defibrillation therapy if the device will not turn on using DC (battery) power and no AC (line) power is available.

Additional Information:

FDA MedWatch Safety Alert. LIFEPAK 20 and LIFEPAK 20e External Defibrillator/Monitors by Physio-Control Inc.: Class I Recall Due To Power Supply Failure. July 2, 2010.
http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm217980.htm


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