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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 576 to 600
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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 17/12/2021
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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 17/12/2021
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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 17/12/2021
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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 17/12/2021
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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 17/12/2021
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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 17/12/2021
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 16/12/2021
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Cancellation or suspensionRegulatory action due to Removal of Excluded Goods, effective 09/12/2021
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Cancellation or suspensionRegulatory action due to Removal of Excluded Goods, effective 09/12/2021
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Cancellation or suspensionRegulatory action due to Nonresponse to a s41JA, effective 09/12/2021
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Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion, effective 01/12/2021
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Cancellation or suspensionRegulatory action due to Nonresponse to a s41JA, effective 27/11/2021
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Cancellation or suspensionRegulatory action due to Nonresponse to a s41JA, effective 27/11/2021
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer., effective 19/11/2021
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Cancellation or suspensionRegulatory action due to Nonresponse to a s41JA, effective 05/11/2021
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Cancellation or suspensionRegulatory action due to Nonresponse to a s41JA, effective 05/11/2021
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Cancellation or suspensionRegulatory action due to Nonresponse to a s41JA, effective 04/11/2021
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Cancellation or suspensionRegulatory action due to Under 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; and it is likely that the person will, within the period of the suspension, be able to take the action necessary to ensure that the kind of device would not cause a potential risk of death, serious illness or serious injury if it were to continue to be included in the Register, effective 03/11/2021
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer., effective 02/11/2021
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer., effective 02/11/2021
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer., effective 02/11/2021
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer., effective 02/11/2021
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer., effective 02/11/2021
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Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion, effective 01/11/2021
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Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion, effective 01/11/2021