Product description

MEDUCORE Easy Automatic External Defibrillator (AED)

See a list of details to help identify the product

Reason the product is recalled

During safety checks, it was discovered that the time allotted for charging the capacitor was insufficient for a full charge to be made.

The hazards to consumers

Potentially life-threatening, or could cause a serious risk to health (Class I)

What consumers should do

Please do not contact the sponsor for further information unless you believe that you have the goods under recall and have not received a recall letter. Refer to the following website for further details:
http://www.tga.gov.au/safety/alerts-device-meducore-defibrillator-111006.htm

Details to help identify the product

Supplier running the recall

Who sold the product

Weinmann Australia Pty Ltd, Ferno Australia Pty Ltd.

Identifying product features

Ferno Australia Pty Ltd is seeking to locate Meducore Easy Automatic External Defibrillators bearing the following serial numbers: 1226, 3163, 3164, 3165, 3167, 3171, 3172, 3176, 3177, 3178, 3182, 3183, 3184, 3185, 3186, 3188, 3189, 3192, 3193, 3199, 3200, 3208

Identifying numbers

Other identifying numbers

Ferno Australia Pty Ltd is seeking to locate Meducore Easy Automatic External Defibrillators bearing the following serial numbers:
1226, 3163, 3164, 3165, 3167, 3171, 3172, 3176, 3177, 3178, 3182, 3183, 3184, 3185, 3186, 3188, 3189, 3192, 3193, 3199, 3200, 3208

Where the product was sold

Australian Capital Territory
New South Wales
Queensland
Victoria
Western Australia

Responsible regulators

Regulators are established or appointed by government. They enforce regulations and rules.

Quote PRA number 2011/12610 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.