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
- 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)
- Voluntary revocation at the request of the manufacturer (39)
- Medical device cancellation - certain devices within an entry (23)
- 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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1910 result(s) found, displaying 1226 to 1250
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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
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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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PHARMACY ACTION ANTISEPTIC CREAM tube (Cancelled from the ARTG under subsection 30(2)(a) of the Act)
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 -
PHARMACY CHOICE ANTISEPTIC CREAM tube (Cancelled from the ARTG under subsection 30(2)(a) of the Act)
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 -
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 Sponsor requested cancellation in writing, effective 17/09/2020
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Cancellation or suspensionRegulatory action due to The certifications made by the sponsor under section 41FD 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 and the sponsor failed to comply with the conditions of inclusion stipulated under paragraph 41FN., effective 16/09/2020
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Cancellation or suspensionRegulatory action due to Devices of that kind are no longer therapeutic goods., effective 16/09/2020
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Cancellation or suspensionRegulatory action due to The response from a Section 41JA notification has informed that the device type is not supplied or imported in Australia, or exported from Australia.The grounds for cancellation apply only to T34L variants of infusion pumps (including T34L, T34L NeoFeed and T34L KID models) and the cancellation is limited under s41GO to vary ARTG 131232 accordingly., effective 08/09/2020
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Cancellation or suspensionRegulatory action due to The certification the sponsor made under section 41FD of the Act in relation to the application for inclusion of the kind of device in the Register was false or misleading in a material particular, effective 04/09/2020
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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 02/09/2020
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