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
- Medicine suspension (87)
- Medicine cancellation (58)
- Medical device cancellation (44)
- Revocation of a TGA issued Conformity Assessment Certificate (19)
- Medical device suspension (14)
- Complementary medicine cancellation (4)
- Revocation of a TGA issued Conformity Assessment Certificate. (3)
- Voluntary revocation at the request of the manufacturer. (1)
Find out more about Cancellations and Suspensions.
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231 result(s) found, displaying 151 to 175
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to a statement made in or in connection with the application for including the kind of device in the Register was false or misleading in a material particular, effective 17/03/2023
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Cancellation or suspensionRegulatory action due to Removal of goods are not therapeutic goods., effective 23-03-2023
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Cancellation or suspensionRegulatory action due to Cancellation of the registration of the goods if the goods do not conform to a standard applicable to the goods, effective 15/02/2023
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Cancellation or suspensionRegulatory action due to Cancellation of the registration of the goods if the goods do not conform to a standard applicable to the goods, effective 15/02/2023
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Cancellation or suspensionRegulatory action due to Cancellation of the entry due to incorrect classification, effective 17/02/2023
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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)., effective 16/02/2023
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Cancellation or suspensionRegulatory action due to As 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)., effective 16/02/2023
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Cancellation or suspensionRegulatory action due to Removal of goods are not therapeutic goods., effective 21-02-2023
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