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DDU-2000 Series Automated External Defibrillator (AED)
Official notice
5 May 2020
Last checked
5 May 2020
An official ACCC notice concerns DDU-2000 Series Automated External Defibrillator (AED). An aborted shock or unexpected delivery may result in patient death under emergency situations. Published 2020-05-05.
What to do now
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.
Recall number
1d23c55b-3aa1-49a6-9127-688e4fb22103
Official notice
2020-05-05
The hazard
The hazard
An aborted shock or unexpected delivery may result in patient death under emergency situations.
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
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Affected products
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Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Source & status
Source & status
Recall details
Recall details
Recall number
Classification
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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