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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 1276 to 1300
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Cancellation or suspensionRegulatory action due to The good had become an exempt good under Schedule 5, Item 8(f) of the Regulations. Exempt goods are not required to be included on the ARTG (paragraph 18(1) of the Act)., effective 18/06/2020
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Cancellation or suspensionRegulatory action due to The good had become an exempt good under Schedule 5, Item 8(f) of the Regulations. Exempt goods are not required to be included on the ARTG (paragraph 18(1) of the Act)., effective 18/06/2020
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Cancellation or suspensionRegulatory action due to The good had become an exempt good under Schedule 5, Item 8(f) of the Regulations. Exempt goods are not required to be included on the ARTG (paragraph 18(1) of the Act)., effective 18/06/2020
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Cancellation or suspensionRegulatory action due to The good had become an exempt good under Schedule 5, Item 8(f) of the Regulations. Exempt goods are not required to be included on the ARTG (paragraph 18(1) of the Act)., effective 18/06/2020
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Cancellation or suspensionRegulatory action due to The good had become an exempt good under Schedule 5, Item 8(f) of the Regulations. Exempt goods are not required to be included on the ARTG (paragraph 18(1) of the Act)., effective 18/06/2020
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Cancellation or suspensionRegulatory action due to The good had become an exempt good under Schedule 5, Item 8(f) of the Regulations. Exempt goods are not required to be included on the ARTG (paragraph 18(1) of the Act)., effective 18/06/2020
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Cancellation or suspensionRegulatory action due to The good had become an exempt good under Schedule 5, Item 8(f) of the Regulations. Exempt goods are not required to be included on the ARTG (paragraph 18(1) of the Act)., effective 18/06/2020
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Cancellation or suspensionRegulatory action due to The good had become an exempt good under Schedule 5, Item 8(f) of the Regulations. Exempt goods are not required to be included on the ARTG (paragraph 18(1) of the Act)., effective 18/06/2020
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Cancellation or suspensionRegulatory action due to The good had become an exempt good under Schedule 5, Item 8(f) of the Regulations. Exempt goods are not required to be included on the ARTG (paragraph 18(1) of the Act)., effective 18/06/2020
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Cancellation or suspensionRegulatory action due to The good had become an exempt good under Schedule 5, Item 8(f) of the Regulations. Exempt goods are not required to be included on the ARTG (paragraph 18(1) of the Act)., effective 18/06/2020
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Cancellation or suspensionRegulatory action due to The sponsor failed to provide information requested under section 41JA of the Act and therefore failed to comply with an automatic condition of inclusion under section 41FN(3)(c) of the Act., effective 16/06/2020
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Cancellation or suspensionRegulatory action due to The sponsor failed to provide information requested by the TGA under section 41JA of the Act. The sponsor therefore failed to comply with an automatic condition of inclusion (s41FN(3)(c) of the Act)., effective 01/06/2020
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Cancellation or suspensionRegulatory action due to The good had become an exempt good under Schedule 5, Item 14 of the Regulations. Exempt goods are not required to be included on the ARTG (paragraph 18(1) of the Act)., effective 26/05/2020
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Cancellation or suspensionRegulatory action due to The good had become an exempt good under Schedule 5, Item 14 of the Regulations. Exempt goods are not required to be included on the ARTG (paragraph 18(1) of the Act)., effective 26/05/2020
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Cancellation or suspensionRegulatory action due to The good had become an exempt good under Schedule 5, Item 14 of the Regulations. Exempt goods are not required to be included on the ARTG (paragraph 18(1) of the Act)., effective 26/05/2020
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Cancellation or suspensionRegulatory action due to The good had become an exempt good under Schedule 5, Item 14 of the Regulations. Exempt goods are not required to be included on the ARTG (paragraph 18(1) of the Act)., effective 26/05/2020
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Cancellation or suspensionRegulatory action due to The good had become an exempt good under Schedule 5, Item 14 of the Regulations. Exempt goods are not required to be included on the ARTG (paragraph 18(1) of the Act)., effective 26/05/2020
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Cancellation or suspensionRegulatory action due to The good had become an exempt good under Schedule 5, Item 14 of the Regulations. Exempt goods are not required to be included on the ARTG (paragraph 18(1) of the Act)., effective 26/05/2020
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Cancellation or suspensionRegulatory action due to The Device was suspended from the Register under section 41GA of the Act, and the period of suspension, applied under subsection 41GC(3) has expired before the suspension was revoked under section 41GD of the Act.The information submitted in response to the suspension is insufficient to remove the grounds for cancellation and fulfil the requirements of the suspension being revoked., effective 20/04/2020
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Cancellation or suspensionRegulatory action due to The device was incorrectly classified as a class I medical device. From the information available the device should be included on the ARTG at a higher classification. Therefore, the certification made by the sponsor under paragraph 41FD(c) of the Act in the application for inclusion is incorrect., effective 14/04/2020
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Cancellation or suspensionRegulatory action due to The device was incorrectly classified as a class I medical device. From the information available the device should be included on the ARTG at a higher classification. Therefore, the certification made by the sponsor under paragraph 41FD(c) of the Act in the application for inclusion is incorrect., effective 01/04/2020
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Cancellation or suspensionRegulatory action due to The sponsor failed to provide information requested by the TGA under section 41JA of the Act. The sponsor therefore failed to comply with an automatic condition of inclusion (s41FN(3)(c) of the Act)., effective 27/03/2020
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Cancellation or suspensionRegulatory action due to The sponsor failed to provide information requested by the TGA under section 41JA of the Act. The sponsor therefore failed to comply with an automatic condition of inclusion (s41FN(3)(c) of the Act)., effective 27/03/2020
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer., effective 13/03/2020
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Cancellation or suspensionRegulatory action due to The sponsor failed to provide evidence to demonstrate that the medical device complies with the applicable provisions of the Essential Principles. The sponsor therefore failed to comply with an automatic condition of inclusion (s41FN(3)(a) of the Act)., effective 24/02/2020