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 1 to 25
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Cancellation or suspensionSuspension from the ARTG under paragraph 41GA(1)(a)
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Cancellation or suspensionSuspension from the ARTG under paragraph 41GA(1)(a)
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Cancellation or suspensionSuspension from the ARTG under paragraph 41GA(1)(a)
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Cancellation or suspensionSuspension from the ARTG under paragraph 41GA(1)(a)
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Cancellation or suspensionUnder subsection 41GA(1)(a) there is a potential risk of death, serious illness or serious injury if the kind of device continues to be included in the Register, effective 21/12/2023
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Cancellation or suspensionSuspension from the ARTG under paragraph 41GA(1)(a)
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Cancellation or suspensionSuspension from the ARTG under paragraph 41GA(1)(a)
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Cancellation or suspensionUnder subsection 41GA(1)(a) there is a potential risk of death, serious illness or serious injury if the kind of device continues to be included in the Register, effective 21/12/2023
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Cancellation or suspensionSuspension from the ARTG under paragraph 41GA(1)(a)
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Cancellation or suspensionUnder subsection 41GA(1)(a) there is a potential risk of death, serious illness or serious injury if the kind of device continues to be included in the Register, effective 21/12/2023
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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 17/12/2023
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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 17/12/2023
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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 17/12/2023
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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 17/12/2023
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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 17/12/2023
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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 17/12/2023
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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 17/12/2023
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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 17/12/2023
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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 17/12/2023
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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 17/12/2023
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer, effective 10/11/2023
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer, effective 10/11/2023
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Cancellation or suspensionRegulatory action under s. 41GC(3): the sponsor has demonstrated that steps have been taken to remove the grounds for cancelling the entry of the kind of device from the Register under s. 41GN and hence extend the period specified in the notice, effective 31 October 2023.
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Cancellation or suspensionRegulatory action under s. 41GC(3): the sponsor has demonstrated that steps have been taken to remove the grounds for cancelling the entry of the kind of device from the Register under section 41GN and hence extend the period specified in the notice, effective 31 October 2023.
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer, effective 26/07/2023
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