AED Product Notices

April 21, 2020

2020 Safety Alert

Defibtech, LLC is initiating a Field Action Notice of certain DDU-2000 series semi-automatic external defibrillators (AEDs) sold under the Lifeline VIEW, Lifeline ECG, and ReviveR VIEW AED brand names. This recall affects only select units shipped within the last several months.

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December 22, 2015

Current AHA/ERC Guidelines

All of Defibtech’s products (those currently being shipping and those updated to the latest software versions) conform to the 2015 American Heart Association (AHA) and European Resuscitation Council (ERC) resuscitation guidelines.

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April 29, 2011

2011 Safety Alert

Defibtech, LLC is initiating a worldwide voluntary recall of certain DDU-100 series semi-automatic external defibrillators (AEDs) sold under the Lifeline AED and ReviveR AED brand names. This recall affects only DDU-100 Series AEDs shipped with 2.004 software or earlier.

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June 4, 2010

2010 Safety Alert

Defibtech, LLC, is initiating a voluntary recall of 5,418 DBP-2800 Battery Packs used in the Lifeline AED® and ReviveR AED™ (semi-automatic external defibrillators). This recall affects all DBP-2800 Battery Packs shipped prior to June 4, 2007.

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March 6, 2007

2007 Safety Alert

Defibtech, LLC, is initiating a voluntary worldwide recall of the Lifeline AED® and ReviveR AED™ (semi-automatic external defibrillators). This recall affects all Lifeline and ReviveR AEDs with software versions 2.002 and earlier.

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