Defibtech, a U.S. manufacturer of life-saving medical equipment, announced today the release of an expansion to their Lifeline VIEW and Lifeline ECG product lines in the United States. The new ...

GUILFORD, Conn.--(BUSINESS WIRE)--Defibtech, LLC is initiating a worldwide voluntary recall of certain DDU-100 series semi-automatic external defibrillators (AEDs) sold under the Lifeline AED and ...

GUILFORD, Conn.--(BUSINESS WIRE)--Defibtech's automated external defibrillators (AEDs) meet the American Heart Association's new "hands-only" CPR guidelines, the company announced today. Unlike many ...

GUILFORD, Conn.--(BUSINESS WIRE)--Defibtech, LLC, a designer and manufacturer of automated external defibrillators (AEDs) and other resuscitation equipment, announced today that it has signed an ...

Last year Defibtech’s vice president Greg Slusser announced that making his company’s Lifeline automated external defibrillators (AEDs) accessible in public venues would provide the greatest benefit ...

March 8, 2007 — A worldwide voluntary recall of 42,000 Lifeline and ReviveR semi-automatic external defibrillators (AEDs) with software versions 2.002 and earlier has been initiated by Defibtech LLC, ...

In December 2024, the United States Senate passed H.R. 6829, the Cardiomyopathy Health Education, Awareness, and Research, and AED Training in the Schools (HEARTS) Act of 2024. The legislation ...

The class I recall announced by the Food and Drug Administration is a worldwide voluntary recall of Lifeline AED and ReviveR AED units shipped with 2.004 software or earlier. May 03, 2011 Owners of at ...