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)
- Medical device cancellation - certain devices within an entry (23)
- Voluntary revocation at the request of the manufacturer (18)
- 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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Cancellation or suspensionRegulatory action due to Nonresponse to a s41JA, effective 05/11/2021
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Cancellation or suspensionRegulatory action due to Nonresponse to a s41JA, effective 04/11/2021
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Cancellation or suspensionRegulatory action due to Under 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; and it is likely that the person will, within the period of the suspension, be able to take the action necessary to ensure that the kind of device would not cause a potential risk of death, serious illness or serious injury if it were to continue to be included in the Register, effective 03/11/2021
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer., effective 02/11/2021
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer., effective 02/11/2021
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer., effective 02/11/2021
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer., effective 02/11/2021
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer., effective 02/11/2021
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Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion, effective 01/11/2021
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Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion, effective 01/11/2021
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Cancellation or suspensionRegulatory action due to Nonresponse to a s41JA, effective 28/10/2021
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Cancellation or suspensionRegulatory action due to Nonresponse to a s41JA, effective 25/10/2021
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Cancellation or suspensionRegulatory action due to Nonresponse to a s41JA, effective 25/10/2021
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Cancellation or suspensionRegulatory action due to Nonresponse to a s41JA, effective 25/10/2021
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Cancellation or suspensionRegulatory action due to Nonresponse to a s41JA, effective 21/10/2021
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Cancellation or suspensionRegulatory action due to Nonresponse to a s41JA, effective 21/10/2021
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Cancellation or suspensionRegulatory action due to Nonresponse to a s41JA, effective 21/10/2021
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Cancellation or suspensionRegulatory action due to Nonresponse to a s41JA, effective 21/10/2021
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Cancellation or suspensionRegulatory action due to Nonresponse to a s41JA, effective 19/10/2021
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Cancellation or suspensionRegulatory action due to Removal of Excluded Goods, effective 14/10/2021
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Cancellation or suspensionRegulatory action due to The Sponsor failed to comply with the notice under section 41JA within a further 10 working days, effective 13/10/2021
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Cancellation or suspensionRegulatory action due to Nonresponse to a s41JA, effective 13/10/2021
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Cancellation or suspensionRegulatory action due to Nonresponse to a s41JA, effective 13/10/2021
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Cancellation or suspensionRegulatory action due to Nonresponse to a s41JA, effective 12/10/2021
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Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion, effective 11/10/2021