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 ...

The Health Products Regulatory Authority has urged users of Defibtech defibrillator pads to immediately check their pads as they may have been labelled with incorrect expiry dates. A number of ...

A warning has been issued in relation to unauthorised labels on some defibrillator pads supplied to the Irish market which display an incorrect expiry date. The Health Products Regulatory Authority ...

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 ...

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 ...

AED manufacturer Defibtech, LLC (Guilford, Conn.) announced Aug. 21 that it has shipped more than 50,000 of its DDU-100 Series AEDs. The defibrillators are marketed under the brand names Lifeline™ and ...

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 ...

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