Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Defibtech DDP-2002: Pediatric Defibrillation Pads For use with AED Models: Recalled by Defibtech, LLC Due to Within the Irish Market, that a Field Safety...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Defibtech, LLC directly.
Affected Products
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.)
Quantity: 22,294 total
Why Was This Recalled?
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
Where Was This Sold?
Ireland
About Defibtech, LLC
Defibtech, LLC has 14 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report