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.
Filter results
You can narrow down the results using the filters.
Find out more about Cancellations and Suspensions.
Search
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 19/03/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 19/03/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 19/03/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 19/03/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 05/03/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 05/03/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 05/03/2021
-
Cancellation or suspensionRegulatory action due to Failure to comply with s41JA within a further 10 days, effective 05/03/2021
-
Cancellation or suspensionRegulatory action due to Failure to comply with s41JA within a further 10 days, effective 05/03/2021
-
Cancellation or suspensionRegulatory action due to Failure to comply with s41JA within a further 10 days, effective 05/03/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 04/03/2021
-
Cancellation or suspensionRegulatory action due to Failure to comply with s41JA within a further 10 days, poor device safety and incorrect certification, effective 04/03/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 01/03/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 01/03/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 24/02/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 22/02/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 22/02/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 22/02/2021
-
Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion and a certification made under 41FD is incorrect in a material particular, effective 22/02/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 22/02/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 22/02/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 19/02/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 19/02/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 19/02/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 19/02/2021