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.
Last updated
Use the filters below to narrow your search.
Filter results
You can narrow down the results using the filters.
Action
- Medicine suspension (74)
- Medical device cancellation (63)
- Medical device cancellation - certain devices within an entry (9)
- Voluntary revocation at the request of the manufacturer (9)
- Revocation of a TGA issued Conformity Assessment Certificate (8)
- Medical device cancellation (7)
- Listed medicine cancellation (3)
- Listed medicine cancellation (3)
- Revocation of medical device suspension (2)
- Revoked medicine suspension (2)
- Alphapharm Pty Ltd (1)
- Complementary medicine cancellation (1)
- Medical device cancellation (1)
- Medical device suspension (1)
- Medicine cancellation (1)
- Suspension from the ARTG under subsection s41GA(1)(b) (1)
Find out more about Cancellations and Suspensions.
Search
191 result(s) found, displaying 126 to 150
-
Cancellation or suspensionWe have cancelled Philips Electronics Australia Ltd, Portable ventilator, electric/47083: Trilogy EV300, INTL-Model IN2200X15B - Under subsection 41GK(1)
-
Cancellation or suspensionWe have cancelled Philips Electronics Australia Ltd - Portable ventilator, electric/47083: Trilogy Evo, O2, International - Model IN2100X15B under s41 GK(1) of the Act
-
Cancellation or suspensionComplementary medicine cancellation from the ARTG, under subsection 30(2) of the Act.
-
Cancellation or suspensionRegulatory action due to , effective 18/04/2024
-
Cancellation or suspensionRegulatory action due to , effective 3/04/2024
-
Cancellation or suspensionWe have cancelled Evolve Therapeutic Aesthetic Supplies Pty Ltd - Hair-removal diode laser system under subsection 41GM(2) of the Act
-
Cancellation or suspensionWe have cancelled ND:YAG - Dermatological Nd:YAG/Frequency-doubled Nd:YAG laser system under subsection 41GM(2) of the Act
-
Cancellation or suspensionWe have cancelled Soma Lasers Australia - Hair-removal diode laser system under subsection 41GM(2) of the Act
-
Cancellation or suspensionThe device is being cancelled due to failure to comply with an automatic condition of inclusion under s. 41FN(5A) of the Act, effective from 25 March 2024.
-
Cancellation or suspensionThe device is being cancelled due to failure to comply with an automatic condition of inclusion under subsection 41FN(5A) of the Act, effective from 25 March 2024.
-
Cancellation or suspensionThe device is being cancelled due to failure to comply with an automatic condition of inclusion under subsection 41FN(5A) of the Act, effective from 25 March 2024.
-
Cancellation or suspensionThe device is being cancelled due to failure to comply with an automatic condition of inclusion under subsection 41FN(5A) of the Act, effective from 25 March 2024.
-
Cancellation or suspensionThe device is being cancelled due to failure to comply with an automatic condition of inclusion under subsection 41FN(5A) of the Act, effective from 25 March 2024.
-
Cancellation or suspensionThe device is being cancelled due to failure to comply with an automatic condition of inclusion under subsection 41FN(5A) of the Act, effective from 25 March 2024.
-
Cancellation or suspensionThe device is being cancelled due to failure to comply with an automatic condition of inclusion under subsection 41FN(5A) of the Act, effective from 25 March 2024.
-
Cancellation or suspensionThe device is being cancelled due to failure to comply with an automatic condition of inclusion under subsection 41FN(5A) of the Act, effective from 25 March 2024.
-
Cancellation or suspensionThe device is being cancelled due to failure to comply with an automatic condition of inclusion under subsection 41FN(5A) of the Act, effective from 25 March 2024.
-
Cancellation or suspensionThe device is being cancelled due to failure to comply with an automatic condition of inclusion under subsection 41FN(5A) of the Act, effective from 25 March 2024.
-
Cancellation or suspensionThe device is being cancelled due to failure to comply with an automatic condition of inclusion under subsection 41FN(5A) of the Act, effective from 25 March 2024.
-
Cancellation or suspensionThe device is being cancelled due to failure to comply with an automatic condition of inclusion under subsection 41FN(5A) of the Act, effective from 25 March 2024.
-
Cancellation or suspensionThe device is being cancelled due to failure to comply with an automatic condition of inclusion under subsection 41FN(5A) of the Act, effective from 25 March 2024.
-
Cancellation or suspensionThe device is being cancelled due to failure to comply with an automatic condition of inclusion under subsection 41FN(5A) of the Act, effective from 25 March 2024.
-
Cancellation or suspensionThe device is being cancelled as the sponsor has failed to comply with an automatic condition of inclusion under subsection 41FN(5A) of the Act, effective from 29 March 2024.
-
Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer, effective
-
Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer, effective
Last updated