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Action
- Medical device cancellation (827)
- Medicine suspension (472)
- Complementary medicine cancellation (203)
- Medical device suspension (86)
- Medicine cancellation (59)
- Revocation of a TGA issued Conformity Assessment Certificate (51)
- Medical device cancellation - certain devices within an entry (22)
- Registered medicine cancellation (12)
- Voluntary revocation at the request of the manufacturer (9)
- Medical device cancellation - requested by the sponsor - certain devices within an entry (8)
- Medical device cancellation (7)
- Listed medicine cancellation (3)
- Listed medicine cancellation (3)
- Revocation of a TGA issued Conformity Assessment Certificate. (3)
- Revocation of medical device suspension (2)
- Revoked medicine suspension (2)
- Medical device cancellation (1)
- Medical device cancellation – certain devices within an entry (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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1780 result(s) found, displaying 451 to 475
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Cancellation or suspensionRegulatory action due to Removal of goods are not therapeutic goods., effective 08-08-2022
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Cancellation or suspensionRegulatory action due to non-response to a s41JA notification, which requires the provision of information or documents
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Cancellation or suspensionRegulatory action due to non-response to a s41JA notification, which requires the provision of information or documents
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Cancellation or suspensionRegulatory action due to non-response to a s41JA notification, which requires the provision of information or documents
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Cancellation or suspensionRegulatory action due to non-response to a s41JA notification, which requires the provision of information or documents
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Cancellation or suspensionRegulatory action due to non-response to a s41JA notification, which requires the provision of information or documents
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Cancellation or suspensionRegulatory action due to non-response to a s41JA notification, which requires the provision of information or documents
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Cancellation or suspensionRegulatory action due to non-response to a s41JA notification, which requires the provision of information or documents
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Cancellation or suspensionRegulatory action due to non-response to a s41JA notification, which requires the provision of information or documents
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Cancellation or suspensionRegulatory action due to non-response to a s41JA notification, which requires the provision of information or documents
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Cancellation or suspensionRegulatory action due to The suspension of the Device from the ARTG was not revoked before the expiry date of the suspension
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Cancellation or suspensionRegulatory action due to Pursuant to section 41GA(1)(b) of the Act, the Secretary has suspended the device as it is likely there are grounds for cancelling the device from the Register under Division 2 (other than under paragraph 41GL(a) or (d) or section 41GM).
The Secretary is satisfied there are grounds for cancelling the device from the Register under subsection 41GN(1)(b) because the Sponsor has failed to comply with the conditions of inclusion set out under subsections 41FN(3)(b) and (c). -
FatBlaster Max (Cancelled from the ARTG under paragraphs 30(1)(e), 30(1)(g) and 30(2)(c) of the Act)
Cancellation or suspensionRegulatory action due to As it appeared to the Secretary that the medicine's label contained an indication that was not proposed to be accepted in relation to the inclusion of the medicine in the Register, the certification made under s.26A(2)(fba) of the Act was incorrect.It appeared to the Secretary that a statement made in, or in connection with, the application for listing of the goods was false or misleading in a material particular.The sponsor failed to comply with a condition of listing under s.28(5)(ab) of the Act (that the goods will not be advertised for an indication other than those accepted in the Register)., effective 16/05/2022 -
Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion, effective 14/04/2022
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Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion, effective 26/03/2022
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 15/03/2022
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer., effective 11/03/2022
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer., effective 11/03/2022
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Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion, effective 11/03/2022
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Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion, effective 09/03/2022
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Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion, effective 09/03/2022
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Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion, effective 09/03/2022
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 09/03/2022
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Cancellation or suspensionRegulatory action due to , effective 09/03/2022
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 09/03/2022