Defibtech, LLC: Medical Device Recall in 2024 - (Recall #: Z-0504-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Defibtech DDP-2001: Adult 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.)

Product Classification:

Class II

Date Initiated: October 14, 2024

Date Posted: December 4, 2024

Recall Number: Z-0504-2025

Event ID: 95594

Reason for Recall:

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

Status: Ongoing

Product Quantity: 22,294 total

Code Information:

UDI-DI: 00815098020447, DDP-2001 adult defibrillation pads, single pack; 30815098020448, DDP-2001 adult defibrillation pads, 10 pairs; 50815098020442, DDP-2001 adult defibrillation pads, 40 pairs

Distribution Pattern:

Ireland

Voluntary or Mandated:

Voluntary: Firm initiated