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
- (-) Complementary medicine cancellation (205)
- Medical device cancellation (851)
- Medicine suspension (506)
- Medical device suspension (88)
- 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)
- Complementary medicine cancellation (2)
- Revoked medicine suspension (2)
- AFT Pharmaceuticals Pty Ltd (1)
- Alphapharm Pty Ltd (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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205 result(s) found, displaying 51 to 75
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Cancellation or suspensionRegulatory action due to The goods were not eligible for listing as they contained a substance in an amount which is not permitted by Schedule 4 of the Therapeutic Goods Regulations.As it appeared to the Secretary that the presentation of the goods was unacceptable, the certification made under s.26A(2)(c) of the Act was incorrect.The sponsor failed to comply with a condition of listing under s.28(5)(ab) of the Act (that the goods would not be advertised for an indication other than those accepted in the Register).The goods do not conform to a standard applicable to the goods., effective 31/07/2019
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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.As there was insufficient information or evidence to support the claims about the product, the certification made under s.26A(2)(j) of the Act was incorrect., effective 22/07/2019
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Cancellation or suspensionRegulatory action due to The Secretary was satisfied that a statement made in, or in connection with, the application for listing of the product was false or misleading in a material particular. It appeared to the Secretary that a certification made by the sponsor under paragraph 26A(2)(ja) of the Act was incorrect., effective 03/06/2019
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Cancellation or suspensionRegulatory action due to It appeared to the Secretary that the presentation of the goods was unacceptable.As there was insufficient evidence to support the indications for the product, the certification made under s.26A(2)(j) of the Act was incorrect.The goods do not conform to a standard applicable to the goods., effective 10/08/2018
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Cancellation or suspensionRegulatory action due to The goods do not conform to a standard applicable to the goods., effective 05/07/2018
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Cancellation or suspensionRegulatory action due to The sponsor failed to comply within 20 working days after a notice was given under section 31 requiring it to provide information or documents about the certifications made in relation to the goods., effective 04/07/2018
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Cancellation or suspensionRegulatory action due to The goods were not eligible for listing as they contained a substance in an amount which is not permitted by Schedule 4 of the Therapeutic Goods Regulations., effective 23/04/2018
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Cancellation or suspensionRegulatory action due to The goods were not eligible for listing as they did not meet the requirements set out in Schedule 4 of the Therapeutic Goods Regulations.The goods were not eligible for listing as they contained a substance in an amount which is not permitted by Schedule 4 of the Therapeutic Goods Regulations., effective 23/04/2018
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Cancellation or suspensionRegulatory action due to The goods were not eligible for listing as they contained a substance in an amount which is not permitted by Schedule 4 of the Therapeutic Goods Regulations., effective 23/04/2018
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Cancellation or suspensionRegulatory action due to The goods were not eligible for listing as they contained a substance in an amount which is not permitted by Schedule 4 of the Therapeutic Goods Regulations., effective 23/04/2018
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Cancellation or suspensionRegulatory action due to As it appeared to the Secretary that the presentation of the goods was unacceptable, the certification made under s.26A(2)(c) of the Act was incorrect.The goods do not conform to a standard applicable to the goods., effective 06/03/2018
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Cancellation or suspensionRegulatory action due to The sponsor failed to comply 20 working days after a notice was given under section 31 requiring it to provide information or documents about the certifications made in relation to the goods., effective 17/01/2018
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Cancellation or suspensionRegulatory action due to The sponsor failed to comply within 20 working days after a notice was given under section 31 requiring it to provide information or documents about the certifications made in relation to the goods., effective 01/11/2017
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Cancellation or suspensionRegulatory action due to The certification under paragraph 26A(2)(j) of the Act, is incorrect (paragraph 30(2)(ba) of the Act) The presentation of the goods in the case of listed goods is unacceptable (paragraph 30(2)(aa) of the Act) The goods have changed so that they have become separate and distinct from the goods in the ARTG (paragraph 30(2)(b) of the Act) The goods do not conform to a standard applicable to the goods (paragraph 30(2)(e) of the Act) The goods do not comply with an applicable provision of the Therapeutic Goods Advertising Code, and/or any other requirement relating to advertising applicable under Part 5-1 or the regulations (paragraph 30(2)(ea) of the Act), effective 22/09/2017
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Cancellation or suspensionRegulatory action due to The sponsor failed to comply within 20 working days after a notice was given under section 31 requiring it to provide information or documents about the certifications made in relation to the goods., effective 14/07/2017
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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 05/06/2017
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Cancellation or suspensionRegulatory action due to The sponsor failed to comply within 20 working days after a notice was given under section 31 requiring it to provide information or documents about the certifications made in relation to the goods., effective 30/05/2017
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Cancellation or suspensionRegulatory action due to The sponsor failed to comply within 20 working days after a notice was given under section 31 requiring it to provide information or documents about the certifications made in relation to the goods., effective 21/03/2017
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Cancellation or suspensionRegulatory action due to The sponsor failed to comply within 20 working days after a notice was given under section 31 requiring it to provide information or documents about the certifications made in relation to the goods., effective 06/02/2017
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Cancellation or suspensionRegulatory action due to The sponsor failed to comply with a condition of listing imposed by the Secretary under s.28(2B) of the Act., effective 01/02/2017
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Cancellation or suspensionRegulatory action due to The sponsor failed to comply with a condition of listing imposed by the Secretary under s.28(2B) of the Act., effective 01/02/2017
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Cancellation or suspensionRegulatory action due to The sponsor failed to comply with a condition of listing imposed by the Secretary under s.28(2B) of the Act., effective 01/02/2017
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Cancellation or suspensionRegulatory action due to As there was insufficient evidence to support the indications for the product, the certification made under s.26A(2)(j) of the Act was incorrect.It appeared to the Secretary that the presentation of the goods was unacceptable., effective 07/12/2016
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Cancellation or suspensionRegulatory action due to As there was insufficient evidence to support the indications for the product, the certification made under s.26A(2)(j) of the Act was incorrect.It appeared to the Secretary that the presentation of the goods was unacceptable., effective 15/11/2016
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Cancellation or suspensionRegulatory action due to The sponsor failed to comply within 20 working days after a notice was given under section 31 requiring it to provide information or documents about the certifications made in relation to the goods., effective 17/10/2016
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