A recall notice for DDU-2000 Series Automated External Defibrillator (AED) supplied by Device Technologies Australia Pty Ltd as an electrical component may cause the product to abort a shock delivery, or reset unexpectedly.
Device Technologies Australia Pty Ltd - DDU-2000 Series Automated External Defibrillator (AED)
PRA No.
2020/18321
Date published
5 May 2020
Product description
DDU-2000 Series Automated External Defibrillator (AED)
DT Product Codes: DCF-E2310-EN and DCF-E2460EN
Serial numbers:
400125196
400125197
400125203
400101350
400101365
ARTG 155076 (Device Technologies Australia Pty Ltd - Defibrillator, semi-automated)
What are the defects?
An electrical component may cause the product to abort a shock delivery, or reset unexpectedly.
What are the hazards?
An aborted shock or unexpected delivery may result in patient death under emergency situations.
What should consumers do?
Device Technologies Australia will contact impacted customers to organise the return and replacement of affected units.
Customers are advised that if alternate units are available for use, please return affected units to Device Technologies and they will be replaced. If no alternate units are available, please inform Device Technologies and continue using the device with caution until replacement is provided.
For more information, contact Device Technologies Customer Service on 1300 338 423.
Supplier
Device Technologies Australia Pty Ltd
Traders who sold this product
Device Technologies Australia
Where the product was sold
New South Wales
Victoria
Responsible regulator
Therapeutic Goods Administration is the responsible regulator for this recall.
Product category
