FDAOctober 14, 2024device

Defibtech DDP-2002: Pediatric Defibrillation Pads For use with AED Models: Lifeline View Auto, lifeline Pro, Lifeline ECG, Lifeline View (DDU-2XXX Series -Indicated for use on victims of sudden cardiac arrest (SCA.)

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Within the Irish Market, that a Field Safety Notice is being issued due to a select number of authorized labelled Defibtech AED Pads, which have had the authorized label removed and an unauthorized label applied, could potentially lead to expired Defibtech AED Pads appearing as though they are within the acceptable shelf life.there is a possibility of hydrogel drying, which may result in poor electrical connection to the patient, which can reduce the energy delivered to the patient

What to do

FDA enforcement status: Ongoing

Brands named

defibtech

UPCs

008150980204541081509802045140815098020452

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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