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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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 01/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 01/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 01/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 01/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 01/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 01/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 01/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 01/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 01/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 01/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 30/09/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 30/09/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 30/09/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 30/09/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 30/09/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 30/09/2020
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Cancellation or suspensionRegulatory action due to The product is not a medical device. Therefore, the certification made by the sponsor under paragraph 41FD(a) of the Act in the application for inclusion is incorrect., effective 28/09/2020
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Cancellation or suspensionRegulatory action due to The product is not a medical device. Therefore, the certification made by the sponsor under paragraph 41FD(a) of the Act in the application for inclusion is incorrect., effective 23/09/2020
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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 18/09/2020
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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 18/09/2020
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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 18/09/2020
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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 18/09/2020
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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 18/09/2020
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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 18/09/2020
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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 18/09/2020