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CellAED: Non-rechargeable public automated external defibrillator

Published: December 18, 2025Recall ID: 546016Category: Medical DevicesCountry: Australia
Australia
Medical DeviceAustraliaAustralia

CellAED: Non-rechargeable public automated external defibrillator

Recalling Firm: TGA

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Reason for Recall / Hazard

The company which has supplied the CellAED devices, RRR Manufacturing Pty Ltd, has gone into liquidation. The liquidators for RRR Manufacturing, are conducting a Critical Recall for all lots of the Ce...

Product Description & Identification

The company which has supplied the CellAED devices, RRR Manufacturing Pty Ltd, has gone into liquidation. The liquidators for RRR Manufacturing, are conducting a Critical Recall for all lots of the CellAED device.

Affected Products

CellAED: Non-rechargeable public automated external defibrillator

Additional Source Details

FieldValue
Guid › #texthttps://www.tga.gov.au/node/546016
Guid › @ is Perma Linktrue
Linkhttps://www.tga.gov.au/safety/recalls-and-other-market-actions/market-actions/cellaed-non-rechargeable-public-automated-external-defibrillator
Pub DateFri, 19 Dec 2025 00:00:00 +1100
Extracted categorydevices

Consumer Action Protocol: What You Should Do Immediately

Safety Steps
1Verify Product Identifiers

Inspect the NDC code, batch number, or control number on your medicine bottle or blister packaging to confirm whether your unit is included.

2Isolate & Discontinue Use

Do not abruptly stop critical prescribed medication without physician advice. Contact your dispensing pharmacist immediately for a safe alternative.

3Claim Free Statutory Remedy

Under statutory consumer protection rules, consumers are entitled to a full refund, certified replacement, or free repair kit without needing the original sales receipt.

4Report Adverse Incidents

If you suffered an injury, illness, or property damage from this product, file an official incident report with regulatory authorities (issuing safety agency).

Your Legal Rights as a Consumer

Recalls are legally binding corrective safety actions overseen by statutory government bodies. Recalling entities are legally prohibited from charging consumers for official safety remedies. If a retailer or dealership refuses your recall remedy, notify the issuing regulatory agency immediately.

Frequently Asked Questions About This Recall

FAQ Guide

Q1:What should I do immediately if I own or bought CellAED: Non-rechargeable public automated external defibrillator?

Check the lot number and NDC on your prescription label. For essential medications, consult your doctor or dispensing pharmacist immediately before abruptly stopping your dose.

Q2:Can I get a full refund or free repair for this recall?

Yes. Recalling manufacturers and retail merchants are required under consumer protection regulations to offer a statutory remedy—typically a full refund, certified repair kit, or replacement unit.

Q3:Do I need my original sales receipt to claim a remedy or refund?

In most recall cases, no receipt is required. Because safety recalls are matters of public health and statutory compliance, retailers and manufacturers routinely issue refunds, store credit, or replacement kits upon presentation of the affected product or lot code.

Q4:Where can I verify official information for this safety alert?

This safety alert is aggregated directly from official regulatory agency records (Government Safety Authority). You can click the 'Official Agency Alert' link on this page to view the primary government notice and contact the manufacturer directly.

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Overview

  • Recalling FirmTGA
  • Risk LevelMedical Device Correction
  • DistributionAustralia
Recall Hazard Severity
Caution (Class III)
Official Agency Alert

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🚨 SAFETY ALERT: TGA - CellAED: Non-rechargeable public automated external defibrillator

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https://therecallfile.com/recalls/cellaed-non-rechargeable-public-automated-external-defibrillator/AU-TGA-546016
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