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)
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)
See a list of details to help identify the product.
Reason the product is recalled
An electrical component may cause the product to abort a shock delivery, or reset unexpectedly.
The hazards to consumers
An aborted shock or unexpected delivery may result in patient death under emergency situations.
What consumers should 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.
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.
Details to help identify the product.
Supplier running the recall
Who sold the product
Device Technologies Australia
Where the product was sold
New South Wales
Victoria
Responsible regulators
Regulators are established or appointed by government. They enforce regulations and rules.
Quote PRA number 2020/18321 when contacting a regulator about this recall.
Recall and remedy questions
Contact the Therapeutic Goods Administration if you have:
- a question about the remedy being offered to you by the business that is responsible for managing this recall, or
- concerns about the way the business is managing this recall.