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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432 result(s) found, displaying 51 to 75
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Cancellation or suspensionRegulatory action due to Under subsection 41GA(1)(b); it is likely that there are grounds for cancelling this kind of device from the ARTG under subsection 41GN(1)(b) & (1)(e)., effective 11/11/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 07/11/2020
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Cancellation or suspensionRegulatory action due to The product is not a therapeutic good/medical device therefore the certification made by the sponsor under paragraph 41FD(a) of the Act in the application for inclusion is incorrect., effective 06/11/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 06/11/2020
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Cancellation or suspensionRegulatory action due to Medical devices of that kind are not being supplied in Australia, imported into Australia or exported from Australia, effective 06/11/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 06/11/2020
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Cancellation or suspensionRegulatory action due to Medical devices of that kind are not being supplied in Australia, imported into Australia or exported from Australia, effective 06/11/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 06/11/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 06/11/2020
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Cancellation or suspensionRegulatory action due to The product is not a therapeutic good/medical device therefore the certification made by the sponsor under paragraph 41FD(a) of the Act in the application for inclusion is incorrect., effective 06/11/2020
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Cancellation or suspensionRegulatory action due to The sponsor failed to comply with a notice under section 41JA of the Act and therefore failed to comply with an automatic condition of inclusion under s41FN(3)(c)of the Act., effective 04/11/2020
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Cancellation or suspensionRegulatory action due to The sponsor failed to provide information requested by the TGA under section 41JA of the Act. The sponsor therefore failed to comply with an automatic condition of inclusion (s41FN(3)(c) of the Act)., effective 03/11/2020
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Cancellation or suspensionRegulatory action due to The sponsor failed to comply with the conditions of inclusion stipulated under paragraph 41FN of the Therapeutic Goods Act 1989., effective 03/11/2020
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Cancellation or suspensionRegulatory action due to The sponsor failed to provide information requested by the TGA under section 41JA of the Act. The sponsor therefore failed to comply with an automatic condition of inclusion (s41FN(3)(c) of the Act)., effective 03/11/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 02/11/2020
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Cancellation or suspensionRegulatory action due to The product is an excluded good for the purposes of the Act, that is, the product is determined not to be a therapeutic good. Therefore the certification made by the sponsor under paragraph 41FD(a) of the Act in the application for inclusion, that the product is a medical device, is incorrect., effective 28/10/2020
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Cancellation or suspensionRegulatory action due to The suspension of the Device from the ARTG was not revoked before the expiry date of the suspension., effective 27/10/2020
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Cancellation or suspensionRegulatory action due to The suspension of the Device from the ARTG was not revoked before the expiry date of the suspension., effective 27/10/2020
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Cancellation or suspensionRegulatory action due to The suspension of the Device from the ARTG was not revoked before the expiry date of the suspension., effective 27/10/2020
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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 22/10/2020
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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 22/10/2020
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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 22/10/2020
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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 22/10/2020
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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 22/10/2020
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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 22/10/2020
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