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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 176 to 200
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Cancellation or suspensionWe have cancelled the Radio-frequency probe cannula from the Australian Register of Therapeutic Goods (ARTG), under section 41GM of the Therapeutic Goods Act 1989.
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Cancellation or suspensionSuspension from the ARTG under paragraph 41GA(1)(a)
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Cancellation or suspensionSuspension from the ARTG under paragraph 41GA(1)(a)
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Cancellation or suspensionSuspension from the ARTG under paragraph 41GA(1)(a)
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Cancellation or suspensionSuspension from the ARTG under paragraph 41GA(1)(a)
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Cancellation or suspensionUnder subsection 41GA(1)(a) there is a potential risk of death, serious illness or serious injury if the kind of device continues to be included in the Register, effective 21/12/2023
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Cancellation or suspensionSuspension from the ARTG under paragraph 41GA(1)(a)
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Cancellation or suspensionSuspension from the ARTG under paragraph 41GA(1)(a)
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Cancellation or suspensionUnder subsection 41GA(1)(a) there is a potential risk of death, serious illness or serious injury if the kind of device continues to be included in the Register, effective 21/12/2023
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Cancellation or suspensionSuspension from the ARTG under paragraph 41GA(1)(a)
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Cancellation or suspensionUnder subsection 41GA(1)(a) there is a potential risk of death, serious illness or serious injury if the kind of device continues to be included in the Register, effective 21/12/2023
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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 17/12/2023
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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 17/12/2023
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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 17/12/2023
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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 17/12/2023
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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 17/12/2023
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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 17/12/2023
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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 17/12/2023
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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 17/12/2023
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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 17/12/2023
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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 17/12/2023
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer, effective 10/11/2023
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer, effective 10/11/2023
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Cancellation or suspensionRegulatory action under s. 41GC(3): the sponsor has demonstrated that steps have been taken to remove the grounds for cancelling the entry of the kind of device from the Register under s. 41GN and hence extend the period specified in the notice, effective 31 October 2023.
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Cancellation or suspensionRegulatory action under s. 41GC(3): the sponsor has demonstrated that steps have been taken to remove the grounds for cancelling the entry of the kind of device from the Register under section 41GN and hence extend the period specified in the notice, effective 31 October 2023.