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
- Medical device cancellation (851)
- Medicine suspension (506)
- Complementary medicine cancellation (205)
- Medical device suspension (87)
- Medicine cancellation (59)
- Revocation of a TGA issued Conformity Assessment Certificate (55)
- Voluntary revocation at the request of the manufacturer (39)
- Medical device cancellation - certain devices within an entry (23)
- Registered medicine cancellation (14)
- Medical device cancellation - requested by the sponsor - certain devices within an entry (8)
- Medical device cancellation (7)
- Listed medicine cancellation (4)
- Listed medicine cancellation (4)
- Revocation of a TGA issued Conformity Assessment Certificate. (3)
- Revocation of medical device suspension (3)
- Revoked medicine suspension (2)
- AFT Pharmaceuticals Pty Ltd (1)
- Alphapharm Pty Ltd (1)
- Complementary Medicine Cancellation (1)
- Complementary medicine cancellation (1)
- Medical device cancellation (1)
- Suspension from the ARTG under subsection s41GA(1)(b) (1)
- Voluntary revocation at the request of the manufacturer. (1)
Find out more about Cancellations and Suspensions.
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1910 result(s) found, displaying 1 to 25
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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 29/01/2026
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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 29/01/2026
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Cancellation or suspensionRegulatory action due to voluntary revocation at the request of the manufacturer, effective 15 May 2025
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Cancellation or suspensionRegulatory action due to voluntary revocation at the request of the manufacturer, effective 23 December 2025
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Cancellation or suspensionRegulatory action due to voluntary revocation at the request of the manufacturer, effective 15 July 2025
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Cancellation or suspensionRegulatory action due to voluntary revocation at the request of the manufacturer, effective 02 December 2025
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Cancellation or suspensionRegulatory action due to voluntary revocation at the request of the manufacturer, effective 15 May 2025
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Cancellation or suspensionRegulatory action due to voluntary revocation at the request of the manufacturer, effective 15 May 2025
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Cancellation or suspensionRegulatory action due to voluntary revocation at the request of the manufacturer, effective 30 May 2025
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Cancellation or suspensionRegulatory action due to voluntary revocation at the request of the manufacturer, effective 8 August 2025
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Cancellation or suspensionRegulatory action due to voluntary revocation at the request of the manufacturer, effective 21 August 2025
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Cancellation or suspensionRegulatory action due to voluntary revocation at the request of the manufacturer, effective 11 August 2025
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Cancellation or suspensionRegulatory action due to voluntary revocation at the request of the manufacturer, effective 11 August 2025
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Cancellation or suspensionRegulatory action due to voluntary revocation at the request of the manufacturer, effective 15 July 2025
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Cancellation or suspensionRegulatory action due to voluntary revocation at the request of the manufacturer, effective 15 July 2025
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Cancellation or suspensionRegulatory action due to voluntary revocation at the request of the manufacturer, effective 15 May 2025
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Cancellation or suspensionRegulatory action due to voluntary revocation at the request of the manufacturer, effective 30 May 2025
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Cancellation or suspensionRegulatory action due to voluntary revocation at the request of the manufacturer, effective 5 May 2025
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Cancellation or suspensionRegulatory action due to voluntary revocation at the request of the manufacturer, effective 3 July 2025
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Cancellation or suspensionRegulatory action due to voluntary revocation at the request of the manufacturer, effective 26 June 2025
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Cancellation or suspensionRegulatory action due to voluntary revocation at the request of the manufacturer, effective 02 December 2025
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Cancellation or suspensionRegulatory action due to voluntary revocation at the request of the manufacturer, effective 31 March 2025
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Cancellation or suspensionRegulatory action due to voluntary revocation at the request of the manufacturer, effective 14 March 2025
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Cancellation or suspensionThe sponsor failed to comply with the 28(7)(c) condition to which the inclusion of the goods is subject (paragraph 30(2)(c) of the Act)
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Cancellation or suspensionThe sponsor failed to comply with the 28(7)(c) condition to which the inclusion of the goods is subject (paragraph 30(2)(c) of the Act)
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