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.
Action
Find out more about Cancellations and Suspensions.
Search
-
Cancellation or suspensionRegulatory action due to The Sponsor failed to comply to the notice under section 41JA within a further 10 working days from the date as specified in that notice., effective 14/01/2020
-
Cancellation or suspensionRegulatory action due to The Sponsor failed to comply to the notice under section 41JA within a further 10 working days from the date as specified in that notice., effective 14/01/2020
-
Cancellation or suspensionRegulatory action due to The Sponsor failed to comply to the notice under section 41JA within a further 10 working days from the date as specified in that notice., effective 14/01/2020
-
Cancellation or suspensionRegulatory action due to The Sponsor failed to comply to the notice under section 41JA within a further 10 working days from the date as specified in that notice., effective 14/01/2020
-
Cancellation or suspensionRegulatory action due to The Sponsor failed to comply to the notice under section 41JA within a further 10 working days from the date as specified in that notice., effective 14/01/2020
-
Cancellation or suspensionRegulatory action due to The Sponsor failed to comply to the notice under section 41JA within a further 10 working days from the date as specified in that notice., effective 14/01/2020
-
Cancellation or suspensionRegulatory action due to The device was incorrectly classified as a class I medical device. From the information available the device should be included on the ARTG at a higher classification. Therefore, the certification made by the sponsor under paragraph 41FD(c) of the Act in the application for inclusion is incorrect., effective 10/01/2020