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.

Following a review by the TGA, complementary medicines can be cancelled from the Australian Register of Therapeutic Goods. These cancellations are made by the Secretary under section 30 of the Therapeutic Goods Act 1989.

Where other actions are taken in relation to safety, a link to the TGA's safety alert will be included in the database under 'Further information'.

The reasons for a cancellation are stated in the database below under 'Grounds for cancellation'.

The heading 'Decision status' provides updated information about cancellation decisions, for example information about any decision to revoke a cancellation decision. It will not appear in every entry.

To find out whether a product is currently authorised for supply in Australia, check the ARTG.

Last updated

20 November 2025

Find out more about Cancellations and Suspensions.

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2023

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231 result(s) found, displaying 101 to 125

AU Q00173 (Revocation of a TGA certificate under section 41ES of the Therapeutic Goods Act 1989)

23 May 2023

Cancellation or suspension

Regulatory action due to Voluntary revocation at the request of the manufacturer, effective 28/02/2023
AU Q00254, AU D00249, AU D00286 (Revocation of a TGA certificate under section 41ES of the Therapeutic Goods Act 1989)

23 May 2023

Cancellation or suspension

Regulatory action due to Voluntary revocation at the request of the manufacturer, effective 17/03/2023
AU Q00365, AU D00441, AU D00711 (Revocation of a TGA certificate under section 41ES of the Therapeutic Goods Act 1989)

23 May 2023

Cancellation or suspension

Regulatory action due to Voluntary revocation at the request of the manufacturer, effective 07/11/2022
AU Q00419, AU D00631 (Revocation of a TGA certificate under section 41ES of the Therapeutic Goods Act 1989)

23 May 2023

Cancellation or suspension

Regulatory action due to Voluntary revocation at the request of the manufacturer, effective 17/03/2023
AU Q00462, AU D00804 (Revocation of a TGA certificate under section 41ES of the Therapeutic Goods Act 1989)

23 May 2023

Cancellation or suspension

Regulatory action due to Voluntary revocation at the request of the manufacturer, effective 07/11/2022
Convection blood/fluid warmer high-flow (Cancelled from the ARTG under subsection 41GK of the Act)

4 May 2023

Cancellation or suspension

Regulatory action due to The suspension of the Device from the ARTG was not revoked before the expiry date of the suspension.
Convection blood/fluid warmer high-flow (Cancelled from the ARTG under subsection 41GK of the Act)

4 May 2023

Cancellation or suspension

Regulatory action due to The suspension of the Device from the ARTG was not revoked before the expiry date of the suspension.
Royal Mom (Cancelled from the ARTG under 30(1C) of the Act)

18 April 2023

Cancellation or suspension

Regulatory action due to The sponsor failed to comply within 20 working days after a notice was given under section 31.
Royal Mom (Cancelled from the ARTG under 30(1C) of the Act)

18 April 2023

Cancellation or suspension

Regulatory action due to The sponsor failed to comply within 20 working days after a notice was given under section 31.
Liver Slim (Cancelled from the ARTG under section 30 of the Act)

14 April 2023

Cancellation or suspension

Regulatory action due to The medicine is not eligible for listing (paragraph 30(1A)(a) of the Act).
Public respirator, single-use (Cancellation from the ARTG under section 9F(2) of the Act)

5 April 2023

Cancellation or suspension

Regulatory action due to Removal of goods are not therapeutic goods., effective 05-04-2023
AMCAL DRY COUGH FORTE pholcodine 4mg/mL oral liquid bottle (Cancellation from the ARTG under s.30(2)(a) of the Act)

29 March 2023

Cancellation or suspension

Regulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
AMCAL DRY COUGH MIXTURE pholcodine 1 mg/mL oral liquid bottle (Cancellation from the ARTG under s.30(2)(a) of the Act)

29 March 2023

Cancellation or suspension

Regulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
APOHEALTH DRY COUGH RELIEF PE & NASAL DECONGESTANT oral liquid bottle (Cancellation from the ARTG under s.30(2)(a) of the Act)

29 March 2023

Cancellation or suspension

Regulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
APOHEALTH DRY TICKLY COUGH RELIEF FORTE pholcodine 4 mg/mL oral liquid bottle (Cancellation from the ARTG under s.30(2)(a) of the Act)

29 March 2023

Cancellation or suspension

Regulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
APOHEALTH DRY TICKLY COUGH RELIEF pholcodine 1mg/mL oral liquid bottle (Cancellation from the ARTG under s.30(2)(a) of the Act)

29 March 2023

Cancellation or suspension

Regulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
APOHEALTH DRY TICKLY COUGH RELIEF pholcodine 1mg/mL oral liquid bottle (new formulation) (Cancellation from the ARTG under s.30(2)(a) of the Act)

29 March 2023

Cancellation or suspension

Regulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
BENADRYL DRY, TICKLY COUGH FORTE pholcodine 4mg/mL oral liquid bottle (Cancellation from the ARTG under s.30(2)(a) of the Act)

29 March 2023

Cancellation or suspension

Regulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
BENADRYL DRY,TICKLY COUGH oral liquid (Cancellation from the ARTG under s.30(2)(a) of the Act)

29 March 2023

Cancellation or suspension

Regulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
BLOOMS THE CHEMIST DRY COUGH RELIEF & NASAL DECONGESTANT PE oral liquid bottle (Cancellation from the ARTG under s.30(2)(a) of the Act)

29 March 2023

Cancellation or suspension

Regulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
CHEMISTS' OWN DRY COUGH FORTE pholcodine 3mg/mL oral liquid bottle (Cancellation from the ARTG under s.30(2)(a) of the Act)

29 March 2023

Cancellation or suspension

Regulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
CHEMISTS' OWN DRY COUGH pholcodine 1mg/mL oral liquid bottle (Cancellation from the ARTG under s.30(2)(a) of the Act)

29 March 2023

Cancellation or suspension

Regulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
CHEMISTS' OWN DRY COUGH PLUS NASAL DECONGESTANT PE oral liquid bottle (Cancellation from the ARTG under s.30(2)(a) of the Act)

29 March 2023

Cancellation or suspension

Regulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
CHEMISTS' OWN DRY COUGH REGULAR pholcodine 1 mg/mL oral liquid bottle (Cancellation from the ARTG under s.30(2)(a) of the Act)

29 March 2023

Cancellation or suspension

Regulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023
CHEMISTS' OWN DRY TICKLY COUGH FORTE pholcodine 4 mg/mL oral liquid bottle (new formulation) (Cancellation from the ARTG under s.30(2)(a) of the Act)

29 March 2023

Cancellation or suspension

Regulatory action due to the product appearing to the Secretary that the quality, safety or efficacy of the goods was unacceptable, effective 29/03/2023

Last updated

20 November 2025

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AU Q00173 (Revocation of a TGA certificate under section 41ES of the Therapeutic Goods Act 1989)

AU Q00254, AU D00249, AU D00286 (Revocation of a TGA certificate under section 41ES of the Therapeutic Goods Act 1989)

AU Q00365, AU D00441, AU D00711 (Revocation of a TGA certificate under section 41ES of the Therapeutic Goods Act 1989)

AU Q00419, AU D00631 (Revocation of a TGA certificate under section 41ES of the Therapeutic Goods Act 1989)

AU Q00462, AU D00804 (Revocation of a TGA certificate under section 41ES of the Therapeutic Goods Act 1989)

Convection blood/fluid warmer high-flow (Cancelled from the ARTG under subsection 41GK of the Act)

Convection blood/fluid warmer high-flow (Cancelled from the ARTG under subsection 41GK of the Act)

Royal Mom (Cancelled from the ARTG under 30(1C) of the Act)

Royal Mom (Cancelled from the ARTG under 30(1C) of the Act)

Liver Slim (Cancelled from the ARTG under section 30 of the Act)

Public respirator, single-use (Cancellation from the ARTG under section 9F(2) of the Act)

AMCAL DRY COUGH FORTE pholcodine 4mg/mL oral liquid bottle (Cancellation from the ARTG under s.30(2)(a) of the Act)

AMCAL DRY COUGH MIXTURE pholcodine 1 mg/mL oral liquid bottle (Cancellation from the ARTG under s.30(2)(a) of the Act)

APOHEALTH DRY COUGH RELIEF PE & NASAL DECONGESTANT oral liquid bottle (Cancellation from the ARTG under s.30(2)(a) of the Act)

APOHEALTH DRY TICKLY COUGH RELIEF FORTE pholcodine 4 mg/mL oral liquid bottle (Cancellation from the ARTG under s.30(2)(a) of the Act)

APOHEALTH DRY TICKLY COUGH RELIEF pholcodine 1mg/mL oral liquid bottle (Cancellation from the ARTG under s.30(2)(a) of the Act)

APOHEALTH DRY TICKLY COUGH RELIEF pholcodine 1mg/mL oral liquid bottle (new formulation) (Cancellation from the ARTG under s.30(2)(a) of the Act)

BENADRYL DRY, TICKLY COUGH FORTE pholcodine 4mg/mL oral liquid bottle (Cancellation from the ARTG under s.30(2)(a) of the Act)

BENADRYL DRY,TICKLY COUGH oral liquid (Cancellation from the ARTG under s.30(2)(a) of the Act)

BLOOMS THE CHEMIST DRY COUGH RELIEF & NASAL DECONGESTANT PE oral liquid bottle (Cancellation from the ARTG under s.30(2)(a) of the Act)

CHEMISTS' OWN DRY COUGH FORTE pholcodine 3mg/mL oral liquid bottle (Cancellation from the ARTG under s.30(2)(a) of the Act)

CHEMISTS' OWN DRY COUGH pholcodine 1mg/mL oral liquid bottle (Cancellation from the ARTG under s.30(2)(a) of the Act)

CHEMISTS' OWN DRY COUGH PLUS NASAL DECONGESTANT PE oral liquid bottle (Cancellation from the ARTG under s.30(2)(a) of the Act)

CHEMISTS' OWN DRY COUGH REGULAR pholcodine 1 mg/mL oral liquid bottle (Cancellation from the ARTG under s.30(2)(a) of the Act)

CHEMISTS' OWN DRY TICKLY COUGH FORTE pholcodine 4 mg/mL oral liquid bottle (new formulation) (Cancellation from the ARTG under s.30(2)(a) of the Act)

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