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Action
- Medical device cancellation (845)
- Medicine suspension (506)
- Complementary medicine cancellation (203)
- Medical device suspension (86)
- Medicine cancellation (59)
- Revocation of a TGA issued Conformity Assessment Certificate (55)
- Medical device cancellation - certain devices within an entry (23)
- Registered medicine cancellation (14)
- Voluntary revocation at the request of the manufacturer (13)
- 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)
- 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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1861 result(s) found, displaying 1 to 25
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Cancellation or suspensionRegulatory action due to voluntary revocation at the request of the manufacturer, effective 18/02/2025
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Cancellation or suspensionRegulatory action due to voluntary revocation at the request of the manufacturer, effective 20/05/2025
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Cancellation or suspensionRegulatory action due to voluntary revocation at the request of the manufacturer, effective 12/02/2025
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Cancellation or suspensionRegulatory action due to voluntary revocation at the request of the manufacturer, effective 5/03/2025
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Cancellation or suspensionRegulatory action due to Under subsection 29D(1)(b); it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) on the basis that the quality of the goods is unacceptable., effective 17/06/2025
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Cancellation or suspensionRegulatory action due to Under subsection 29D(1)(b); it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) on the basis that the quality of the goods is unacceptable., effective 17/06/2025
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Cancellation or suspensionRegulatory action due to Under subsection 29D(1)(b); it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) on the basis that the quality of the goods is unacceptable., effective 17/06/2025
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Cancellation or suspensionRegulatory action due to Under subsection 29D(1)(b); it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) on the basis that the quality of the goods is unacceptable., effective 17/06/2025
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Cancellation or suspensionRegulatory action due to Under subsection 29D(1)(b); it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) on the basis that the quality of the goods is unacceptable., effective 17/06/2025
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Cancellation or suspensionRegulatory action due to Under subsection 29D(1)(b); it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) on the basis that the quality of the goods is unacceptable., effective 17/06/2025
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Cancellation or suspensionRegulatory action due to Under subsection 29D(1)(b); it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) on the basis that the quality of the goods is unacceptable., effective 17/06/2025
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Cancellation or suspensionRegulatory action due to Under subsection 29D(1)(b); it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) on the basis that the quality of the goods is unacceptable., effective 17/06/2025
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Cancellation or suspensionCancelled from the ARTG under subsection 30(2)(a) of the Act. It appeared to the Secretary that the quality, safety or efficacy of the goods was unacceptable.
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Cancellation or suspensionCancelled from the ARTG under subsection 30(2)(a) of the Act. It appeared to the Secretary that the quality, safety or efficacy of the goods was unacceptable.
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer, effective 18/02/2025
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer, effective 10/01/2025
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer, effective 14/01/2025
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer, effective 12/02/2025
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Cancellation or suspensionCancellation of the entry as the sponsor did not comply with a condition to which the inclusion of the Good is subject, and the Good does not conform to a standard applicable to the Good.
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Cancellation or suspensionCancellation of the entry as the sponsor did not comply with the conditions of inclusion to which the inclusion of the Device in the ARTG is subject to per paragraph 41GN(1)(b) of the Act.
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Cancellation or suspensionCancellation of the entry due to incorrect classification of the device
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Cancellation or suspensionCancellation of the entry due to incorrect classification of the device
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Cancellation or suspensionCancellation of the entry due to incorrect classification of the device
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Cancellation or suspensionCancellation of the entry due to incorrect classification of the device
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Cancellation or suspensionCancellation of the entry due to incorrect classification of the device