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.
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Action
- Medicine suspension (87)
- Medicine cancellation (58)
- Medical device cancellation (44)
- Revocation of a TGA issued Conformity Assessment Certificate (19)
- Medical device suspension (14)
- Complementary medicine cancellation (4)
- Revocation of a TGA issued Conformity Assessment Certificate. (3)
- Voluntary revocation at the request of the manufacturer. (1)
Find out more about Cancellations and Suspensions.
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231 result(s) found, displaying 76 to 100
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Cancellation or suspensionRegulatory action due to the sponsor failing to comply with an automatic condition of inclusion under subsection 41FN(5A) of the Therapeutic Goods Act 1989.
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Cancellation or suspensionRegulatory action due to Failure to comply with conditions of inclusion and provide evidence to demonstrate that the Device complies with the applicable provisions of the Act and the Regulations, effective 6 June 2023
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Cancellation or suspensionRegulatory action due to Failure to respond with information requested under s41JA to provide evidence to demonstrate that the Device complies with the applicable provisions of the Act and the Regulations, effective 10 May 2023
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Cancellation or suspensionCancelled from the ARTG under 30(1C) of the Act
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Cancellation or suspensionRegulatory action due to Under subsection 29D(1)(b); it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) on the basis that the quality of the goods is unacceptable., effective 17-06-2023
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Cancellation or suspensionRegulatory action due to Under subsection 29D(1)(b); it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) on the basis that the quality of the goods is unacceptable., effective 17-06-2023
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Cancellation or suspensionRegulatory action due to Under subsection 29D(1)(b); it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) on the basis that the quality of the goods is unacceptable., effective 17-06-2023
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Cancellation or suspensionRegulatory action due to Under subsection 29D(1)(b); it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) on the basis that the quality of the goods is unacceptable., effective 17-06-2023
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Cancellation or suspensionRegulatory action due to Under subsection 29D(1)(b); it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) on the basis that the quality of the goods is unacceptable., effective 17-06-2023
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Cancellation or suspensionRegulatory action due to Under subsection 29D(1)(b); it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) on the basis that the quality of the goods is unacceptable., effective 17-06-2023
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Cancellation or suspensionRegulatory action due to Under subsection 29D(1)(b); it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) on the basis that the quality of the goods is unacceptable., effective 17-06-2023
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Cancellation or suspensionRegulatory action due to Under subsection 29D(1)(b); it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) on the basis that the quality of the goods is unacceptable., effective 17-06-2023
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Cancellation or suspensionRegulatory action due to Under subsection 29D(1)(b); it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) on the basis that the quality of the goods is unacceptable., effective 17-06-2023
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Cancellation or suspensionRegulatory action due to Under subsection 29D(1)(b); it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) on the basis that the quality of the goods is unacceptable., effective 17-06-2023
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Cancellation or suspensionRegulatory action due to Under subsection 29D(1)(b); it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) on the basis that the quality of the goods is unacceptable., effective 17-06-2023
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Cancellation or suspensionRegulatory action due to As the sponsor did not provide information to substantiate compliance with the Essential Principles, the sponsor failed to comply with a condition to which inclusion of the kind of device in the ARTG was subject under s.41FN(3)(a)., effective 5 June 2023
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Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion, effective 09-06-2023
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Cancellation or suspensionRegulatory action due to Removal of goods are not therapeutic goods., effective 26-05-2023
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer, effective 03/05/2022
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer, effective 06/10/2022
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer, effective 17/03/2023
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer, effective 06/10/2022
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer, effective 24/03/2023
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer, effective 06/10/2022
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer, effective 13/04/2023
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