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
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.