Cancellations and suspensions
This database records details of medicines and medical devices that have been cancelled or suspended, and no longer appear in the ARTG.
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- (-) Complementary medicine cancellation (203)
- (-) Medicine cancellation (59)
- (-) Alphapharm Pty Ltd (1)
- Medical device cancellation (845)
- Medicine suspension (506)
- Medical device suspension (86)
- Revocation of a TGA issued Conformity Assessment Certificate (55)
- Medical device cancellation - certain devices within an entry (23)
- Registered medicine cancellation (14)
- Voluntary revocation at the request of the manufacturer (13)
- 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)
- AFT Pharmaceuticals Pty Ltd (1)
- Complementary Medicine Cancellation (1)
- Medical device cancellation (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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263 result(s) found, displaying 1 to 25
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Cancellation or suspensionRegulatory action due to , effective 17/12/2024
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Cancellation or suspensionRegulatory action due to incorrect certification under paragraph 26A(2)(a) of the Act (paragraph 30(1)(e) of the Act), the medicine is not eligible for listing, in accordance with paragraph 30(1A)(a) of the Act.
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Cancellation or suspensionWe have cancelled the medicine Hangover Relief 304293, from the Australian Register of Therapeutic Goods (ARTG) under 30(2) of the Therapeutic Goods Act 1989. Effective 24/1/24.
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Cancellation or suspensionWe have cancelled the Deep Lung Support medicine under paragraph 30(2)(c) of the Therapeutic Goods Act 1989.
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Cancellation or suspensionRegulatory action; it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) of the Act on the basis that the quality of the goods is unacceptable., effective 01-08-2023
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Cancellation or suspensionCancelled from the ARTG under 30(1C) of the Act
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Cancellation or suspensionRegulatory action due to The sponsor failed to comply within 20 working days after a notice was given under section 31.
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Cancellation or suspensionRegulatory action due to The sponsor failed to comply within 20 working days after a notice was given under section 31.
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Cancellation or suspensionRegulatory action due to The medicine is not eligible for listing (paragraph 30(1A)(a) of the Act).
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
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Cancellation or suspensionRegulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023