Product description

GE Healthcare TruSat Pulse Oximeter (used for transcutaneous measurment of oxygen saturation)

See a list of details to help identify the product

Reason the product is recalled

The external power supply does not conform with current safety standards. It is possible that the external power supply could leak electrical current.

The hazards to consumers

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

What consumers should do

Home care patients will be contacted individually by their treating doctor.

Details to help identify the product

Supplier running the recall

GE Healthcare Australia Pty Ltd

Identifying product features

Reference numbers: 6051-0000-190, 6051-0000-191, 6051-0000-192 and 6051-0000-193 ARTG number 139421

Identifying numbers

Other identifying numbers

Reference numbers:
6051-0000-190,
6051-0000-191,
6051-0000-192 and
6051-0000-193

ARTG number 139421

Where the product was sold

New South Wales
Northern Territory
Queensland
Victoria
Western Australia

Responsible regulators

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

Quote PRA number 2010/11551 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.