Print version of this report
TGA Action ID RC-2025-RN-01072-1
Type of Product Medical Device
Product Name/Description CellAED - Non-rechargeable public automated external defibrillator

Certificate Number DV-2021-MC-17156-1
ARTG Number 375339
Action Type Recall
Action Level Consumer
Hazard Classification Class I
Reason for the Action The company which has supplied the CellAED devices, RRR Manufacturing, has gone into administration. Hall Chadwick, the liquidators for RRR Manufacturing, are conducting a Critical Recall for all lots of the CellAED device.

As the company has entered administration, they can no longer support products in the market. Without ongoing support such as maintenance, servicing and handling of faults there is an increased risk of safety or performance problems, meaning the device may not work as intended in an emergency.
Instructions for Customers/Users 1. Customers should not use this device.
2. Consult a licensed waste disposal specialist or an approved waste disposal centre to ensure safe and compliant disposal of the device.
3. No replacement stock will be available.
4. To make a claim for any money owed to you, contact RRRenquiries@hallchadwick.com.au.

This action has been finalised on 10/4/2026.
Action Commencement Date 18/12/2025
Responsible Entity RRR Manufacturing Pty Ltd
Contact Information (02) 9263 2652 - Hall Chadwick