Defibtech Lifeline and ReviveR Automated External Defibrillators (AEDs): Recall
MedSun: Newsletter #61, June 2011

FDA MedWatch Safety Alert

Devices subject to this recall include Model DDU-100 series with software version 2.004 or earlier, sold under the brand names Lifeline and ReviveR. AEDs using software version 2.004 or earlier may cause the device to cancel shock during the charging process.

Additional Information:

FDA MedWatch Safety Alert. Defibtech Lifeline and ReviveR Automated External Defibrillators (AEDs): Recall. May 10, 2011.
http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm254929.htm


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