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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 976 to 1000
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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 17/12/2020
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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 17/12/2020
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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 17/12/2020
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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 17/12/2020
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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 17/12/2020
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Cancellation or suspensionRegulatory action due to Non response following s41JA, effective 17/12/2020
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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 17/12/2020
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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 17/12/2020
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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 09/12/2020
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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 09/12/2020
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Cancellation or suspensionRegulatory action due to The product is not a medical device. Therefore, the certification made by the sponsor under paragraph 41FD(a) of the Act in the application for inclusion is incorrect, effective 09/12/2020
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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 08/12/2020
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Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion, effective 07/12/2020
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Cancellation or suspensionRegulatory action due to Non response following a s41JA, effective 03/12/2020
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Cancellation or suspensionRegulatory action due to Non response following a s41JA, effective 03/12/2020
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Cancellation or suspensionRegulatory action due to Non response following a s41JA, effective 03/12/2020
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Cancellation or suspensionRegulatory action due to Non response following a s41JA, effective 03/12/2020
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Cancellation or suspensionRegulatory action due to Non response following a s41JA, effective 03/12/2020
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Cancellation or suspensionRegulatory action due to Non response following a s41JA, effective 03/12/2020
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Cancellation or suspensionRegulatory action due to The sponsor failed to demonstrate that the Device complies with Essential Principles 1,3,6,13, 14 and 15., effective 02/12/2020
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer., effective 01/12/2020
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Cancellation or suspensionRegulatory action due to The Sponsor failed to comply with the notice under section 41JA within a further 10 working days., effective 26/11/2020
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Cancellation or suspensionRegulatory action due to The product is not a medical device therefore the certifications made under section 41FD of the Act at the time of application are incorrect., effective 25/11/2020
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Cancellation or suspensionRegulatory action due to Under subsection 41GA(1)(b); it is likely that there are grounds for cancelling this kind of device from the ARTG under subsection 41GN(1)(b) & (1)(e)., effective 24/11/2020
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Cancellation or suspensionRegulatory action due to The sponsor failed to respond to a request for information and therefore failed to comply with an automatic condition of inclusion., effective 23/11/2020