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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 351 to 375
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Cancellation or suspensionRegulatory action due to Removal of goods are not therapeutic goods., effective 21-02-2023
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Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion, effective 20-02-2023
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Cancellation or suspensionRegulatory action due to Removal of goods are not therapeutic goods, effective 26/09/2022
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Cancellation or suspensionRegulatory action due to Non response to a s41JA request for information, effective 13/09/2022
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Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion, effective 23/12/2022
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Cancellation or suspensionRegulatory action due to Non response to a s41JA request for information, effective 13/09/2022
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Cancellation or suspensionRegulatory action due to Non response to a s41JA request for information, effective 4/10/2022
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Cancellation or suspensionRegulatory action due to Non response to a s41JA request for information, effective 4/10/2022
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Cancellation or suspensionRegulatory action due to Removal of goods are not therapeutic goods, effective 12/09/2022
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Cancellation or suspensionRegulatory action due to Removal of goods are not therapeutic goods, effective 22/12/2022
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Cancellation or suspensionRegulatory action due to Non response to a s41JA request for information, effective 13/09/2022
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Cancellation or suspensionRegulatory action due to Non response to a s41JA request for information, effective 4/10/2022
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Cancellation or suspensionRegulatory action due to Non response to a s41JA request for information, effective 18/10/2022
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Cancellation or suspensionRegulatory action due to Non response to a s41JA request for information, effective 25/10/2022
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Cancellation or suspensionRegulatory action due to Non response to a s41JA request for information, effective 16/01/2023
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Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion, effective 20/09/2022
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Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion, effective 21/09/2022
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Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion, effective 2/11/2022
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Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion, effective 8/11/2022
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Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion, effective 14/11/2022
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Cancellation or suspensionRegulatory action due to Removal of goods are not therapeutic goods, effective 28/09/2022
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Cancellation or suspensionRegulatory action due to Non response to a s41JA request for information, effective 18/10/2022
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Cancellation or suspensionRegulatory action due to Non response to a s41JA request for information, effective 23/09/2022
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Cancellation or suspensionRegulatory action due to failure to comply with a condition of inclusion, effective 25/01/2023
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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 29/01/2023