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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- 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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1889 result(s) found, displaying 651 to 675
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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 29/01/2022
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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 29/01/2022
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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 29/01/2022
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Cancellation or suspensionRegulatory action due to Removal of Excluded Goods, effective 28/01/2022
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Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion, effective 28/01/2022
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Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion, effective 24/01/2022
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Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion, effective 24/01/2022
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Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion, effective 24/01/2022
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Cancellation or suspensionRegulatory action due to Removal of Excluded Goods, effective 21/01/2022
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 19/01/2022
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 19/01/2022
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 19/01/2022
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Cancellation or suspensionRegulatory action due to The sponsor did not provide information to substantiate compliance with the Essential Principles, the sponsor failed to comply with a condition to which inclusion of the kind of device in the ARTG was subject under s.41FN(3)(a).The sponsor was notified of the cancellation under s.41GN(1)(b) on 7 December 2021. Prior to the cancellation taking effect on 14 January 2022, 20 working days after the notification of the cancellation (s.41GQ), the sponsor requested the cancellation of the ARTG inclusion under s.41GL(d)., effective 14/01/2022
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Cancellation or suspensionRegulatory action due to It appeared to the Secretary that the quality, safety or efficacy of the goods was unacceptable., effective 07/01/2022
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Cancellation or suspensionRegulatory action due to Failure to comply with conditions of inclusion, effective 07/01/2022
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Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion, the safety or performance of the Device is unacceptable and Certification made under 41FD(d) is incorrect, effective 04/01/2022
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Cancellation or suspensionRegulatory action due to Failure to comply with conditions of inclusion, effective 04/01/2022
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 04/01/2022
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 01/01/2022
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Cancellation or suspensionRegulatory action due to It appeared to the Secretary that the quality, safety or efficacy of the goods was unacceptable., effective 21/12/2021
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Cancellation or suspensionRegulatory action due to Certification made under 41FD(d) is incorrect, effective 20/12/2021
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Cancellation or suspensionRegulatory action due to Removal of Excluded Goods, effective 20/12/2021
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 20/12/2021
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Cancellation or suspensionRegulatory action due to Removal of Excluded Goods, effective 20/12/2021
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Cancellation or suspensionRegulatory action due to Removal of Excluded Goods, effective 20/12/2021
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