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 1151 to 1175
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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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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 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 20/10/2020
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Cancellation or suspensionRegulatory action due to Non response to s41JA, effective 19/10/2020
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Cancellation or suspensionRegulatory action due to The sponsor failed to provide information to comply with Essential principles of s41FN(3)(a), failed to provide evidence that device complies with conformity assessment procedures of s41FN(3)(b) and certifications made by the sponsor under section s41FC(2) of the Therapeutic Goods Act 1989 in relation to the inclusion of the kind of device in the ARTG are incorrect in a material particular., effective 16/10/2020
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Cancellation or suspensionRegulatory action due to The medical device is incorrectly classified. Therefore, the certification made by the sponsor under paragraph 41FD(c) of the Act in the application for inclusion is incorrect., effective 14/10/2020
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Cancellation or suspensionRegulatory action due to Sponsor requested in writing the cancellation of the kind of device from the Register, effective 12/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 12/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 12/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 12/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 12/10/2020
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Cancellation or suspensionRegulatory action due to The safety and performance of the kind of device is unacceptable, effective 12/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 12/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 09/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 09/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 09/10/2020
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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 07/10/2020
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Cancellation or suspensionRegulatory action due to The sponsor failed to provide information requested by the Secretary therefore the sponsor failed to comply with an automatic condition of inclusion under paragraph 41FN(3)(c) of the Act., effective 07/10/2020
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