Defibtech Recalls LifeLine and Reviver AEDs
Defibtech initiated a voluntary recall of two semi-automatic External Defibrillators (AEDs): ReviveR and Lifeline on February 22nd. The recall includes devices running on software version 2.002 and earlier versions. Software problems may prevent recognition of a low battery because of a malfunction in the self-test software. A device with a low battery may not be able to deliver the appropriate shock.
Defibtech is providing a maintenance procedure to determine device functionality. Software upgrades will also be provided, expected to be available in ten weeks. Affected customers can contact the company at techsupport@defibtech.com, 1-877-453-4507 or 1-203-453-4507.
AEDs are indicated for use in patients with cardiac arrest. Normal heart rhythm is restored by a shock delivered to the heart directly. The device assesses the patient’s heart rhythm to determine whether a shock is required.
Related story: JAMA, FDA Look at Advisories Issued for AEDs.
March 8, 2007 Related topics: Product Recalls, Monitoring, Emergency, Cardiology