Cancellations and suspensions

This database records details of medicines and medical devices that have been cancelled or suspended, and no longer appear in the ARTG.

Following a review by the TGA, complementary medicines can be cancelled from the Australian Register of Therapeutic Goods. These cancellations are made by the Secretary under section 30 of the Therapeutic Goods Act 1989.

Where other actions are taken in relation to safety, a link to the TGA's safety alert will be included in the database under 'Further information'.

The reasons for a cancellation are stated in the database below under 'Grounds for cancellation'.

The heading 'Decision status' provides updated information about cancellation decisions, for example information about any decision to revoke a cancellation decision. It will not appear in every entry.

To find out whether a product is currently authorised for supply in Australia, check the ARTG.

Last updated

20 November 2025

Find out more about Cancellations and Suspensions.

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2022

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152 result(s) found, displaying 26 to 50

Mask, surgical, single use (Cancellation from the ARTG under section 9F(2) of the Act)

14 October 2022

Cancellation or suspension

Regulatory action due to removal of Excluded Goods
Mask, surgical, single use (Cancellation from the ARTG under section 9F(2) of the Act)

14 October 2022

Cancellation or suspension

Regulatory action due to removal of Excluded Goods
Mask, surgical, single use (Cancellation from the ARTG under subsection 41GM(1) of the Act)

14 October 2022

Cancellation or suspension

Regulatory action due to non response to a s41JA notification, which requires the provision of information or documents
Mask, surgical, single use (Cancellation from the ARTG under subsection 41GM(1) of the Act)

14 October 2022

Cancellation or suspension

Regulatory action due to non-response to a s41JA notification, which requires the provision of information or documents
Mask, surgical, single use (Cancellation from the ARTG under subsection 41GM(1) of the Act)

14 October 2022

Cancellation or suspension

Regulatory action due to non-response to a s41JA notification, which requires the provision of information or documents
Mask, surgical, single use (Cancellation from the ARTG under subsection 41GM(1) of the Act)

14 October 2022

Cancellation or suspension

Regulatory action due to non-response to a s41JA notification, which requires the provision of information or documents
Mask, surgical, single use (Cancellation from the ARTG under subsection 41GM(1) of the Act)

14 October 2022

Cancellation or suspension

Regulatory action due to non-response to a s41JA notification, which requires the provision of information or documents
Mask, surgical, single use (Cancellation from the ARTG under subsection 41GN(1) of the Act)

14 October 2022

Cancellation or suspension

Regulatory action due to failure to comply with a condition of inclusion
Mask, surgical, single use (Cancellation from the ARTG under subsection 41GN(1) of the Act)

14 October 2022

Cancellation or suspension

Regulatory action due to failure to comply with a condition of inclusion
Public respirator, single-use (Cancellation from the ARTG under section 9F(2) of the Act)

14 October 2022

Cancellation or suspension

Regulatory action due to removal of Excluded Goods
Public respirator, single-use (Cancellation from the ARTG under section 9F(2) of the Act)

14 October 2022

Cancellation or suspension

Regulatory action due to Removal of Excluded Goods
Public respirator, single-use (Cancellation from the ARTG under subsection 41GM(2) of the Act)

14 October 2022

Cancellation or suspension

Regulatory action due to medical devices of that kind are not being supplied in Australia, imported into Australia or exported from Australia
Surgical/medical respirator, single-use (Cancellation from the ARTG under subsection 41GM(2) of the Act)

14 October 2022

Cancellation or suspension

Regulatory action due to medical devices of that kind not being supplied in Australia, imported into Australia or exported from Australia
Convection blood/fluid warmer high-flow (Suspension from the ARTG under subsection 41GA(1)(b) of the Act)

13 October 2022

Cancellation or suspension

Regulatory action under subsection 41GN(1)(b) because the Sponsor has failed to comply with the conditions of inclusion set out under subsections 41FN(3)(a) & (3)(b)
Convection blood/fluid warmer high-flow (Suspension from the ARTG under subsection 41GA(1)(b) of the Act)

13 October 2022

Cancellation or suspension

Regulatory action under subsection 41GN(1)(b) because the Sponsor has failed to comply with the conditions of inclusion set out under subsections 41FN(3)(a) & (3)(b)
Floradix Liquid Magnesium 250ml (Cancellation from the ARTG under paragraph 30(2)(ba) of the Act)

13 October 2022

Cancellation or suspension

Regulatory action due to The certification made by the sponsor under paragraph 26A(2)d) of the Act was incorrect (paragraph 30(2)(ba) of the Act).
CAD/CAM unit, dental, chairside (Cancellation from the ARTG under subsection 41GN(1) of the Act)

20 September 2022

Cancellation or suspension

Regulatory action due to non-response to a s41JA notification, which requires the provision of information or documents
Clinical data collection/management information application software (Cancellation from the ARTG under subsection 41GN(1) of the Act)

20 September 2022

Cancellation or suspension

Regulatory action due to non-response to a s41JA notification, which requires the provision of information or documents
Aerosol face mask, rebreathing (Cancellation from the ARTG under section 9F(2) of the Act)

8 August 2022

Cancellation or suspension

Regulatory action due to Removal of goods are not therapeutic goods., effective 08-08-2022
Mask, surgical, single use (Cancellation from the ARTG under subsection 41GN(1) of the Act)

2 August 2022

Cancellation or suspension

Regulatory action due to non-response to a s41JA notification, which requires the provision of information or documents
Mask, surgical, single use (Cancellation from the ARTG under subsection 41GN(1) of the Act)

2 August 2022

Cancellation or suspension

Regulatory action due to non-response to a s41JA notification, which requires the provision of information or documents
Mask, surgical, single use (Cancellation from the ARTG under subsection 41GN(1) of the Act)

2 August 2022

Cancellation or suspension

Regulatory action due to non-response to a s41JA notification, which requires the provision of information or documents
Mask, surgical, single use (Cancellation from the ARTG under subsection 41GN(1) of the Act)

2 August 2022

Cancellation or suspension

Regulatory action due to non-response to a s41JA notification, which requires the provision of information or documents
Mask, surgical, single use (Cancellation from the ARTG under subsection 41GN(1) of the Act)

2 August 2022

Cancellation or suspension

Regulatory action due to non-response to a s41JA notification, which requires the provision of information or documents
Mask, surgical, single use (Cancellation from the ARTG under subsection 41GN(1) of the Act)

2 August 2022

Cancellation or suspension

Regulatory action due to non-response to a s41JA notification, which requires the provision of information or documents

Last updated

20 November 2025

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Mask, surgical, single use (Cancellation from the ARTG under section 9F(2) of the Act)

Mask, surgical, single use (Cancellation from the ARTG under section 9F(2) of the Act)

Mask, surgical, single use (Cancellation from the ARTG under subsection 41GM(1) of the Act)

Mask, surgical, single use (Cancellation from the ARTG under subsection 41GM(1) of the Act)

Mask, surgical, single use (Cancellation from the ARTG under subsection 41GM(1) of the Act)

Mask, surgical, single use (Cancellation from the ARTG under subsection 41GM(1) of the Act)

Mask, surgical, single use (Cancellation from the ARTG under subsection 41GM(1) of the Act)

Mask, surgical, single use (Cancellation from the ARTG under subsection 41GN(1) of the Act)

Mask, surgical, single use (Cancellation from the ARTG under subsection 41GN(1) of the Act)

Public respirator, single-use (Cancellation from the ARTG under section 9F(2) of the Act)

Public respirator, single-use (Cancellation from the ARTG under section 9F(2) of the Act)

Public respirator, single-use (Cancellation from the ARTG under subsection 41GM(2) of the Act)

Surgical/medical respirator, single-use (Cancellation from the ARTG under subsection 41GM(2) of the Act)

Convection blood/fluid warmer high-flow (Suspension from the ARTG under subsection 41GA(1)(b) of the Act)

Convection blood/fluid warmer high-flow (Suspension from the ARTG under subsection 41GA(1)(b) of the Act)

Floradix Liquid Magnesium 250ml (Cancellation from the ARTG under paragraph 30(2)(ba) of the Act)

CAD/CAM unit, dental, chairside (Cancellation from the ARTG under subsection 41GN(1) of the Act)

Clinical data collection/management information application software (Cancellation from the ARTG under subsection 41GN(1) of the Act)

Aerosol face mask, rebreathing (Cancellation from the ARTG under section 9F(2) of the Act)

Mask, surgical, single use (Cancellation from the ARTG under subsection 41GN(1) of the Act)

Mask, surgical, single use (Cancellation from the ARTG under subsection 41GN(1) of the Act)

Mask, surgical, single use (Cancellation from the ARTG under subsection 41GN(1) of the Act)

Mask, surgical, single use (Cancellation from the ARTG under subsection 41GN(1) of the Act)

Mask, surgical, single use (Cancellation from the ARTG under subsection 41GN(1) of the Act)

Mask, surgical, single use (Cancellation from the ARTG under subsection 41GN(1) of the Act)

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