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Action
- Medical device cancellation (753)
- Medicine suspension (354)
- Complementary medicine cancellation (201)
- Medical device suspension (71)
- Medicine cancellation (56)
- Revocation of a TGA issued Conformity Assessment Certificate (36)
- Medical device cancellation - certain devices within an entry (14)
- Registered medicine cancellation (12)
- Medical device cancellation - requested by the sponsor - certain devices within an entry (8)
Find out more about Cancellations and Suspensions.
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1505 result(s) found, displaying 1 to 25
- Cancellation or suspensionAU D00226, AU D00380, AU D00471, AU D00657, AU D00736 (Revocation of a TGA certificate under section 41ES of the Therapeutic Goods Act 1989)Regulatory action due to Voluntary revocation at the request of the manufacturer, effective 03/05/2022
- Cancellation or suspensionAU D00853 (Revocation of a TGA certificate under section 41ES of the Therapeutic Goods Act 1989)Regulatory action due to Voluntary revocation at the request of the manufacturer, effective 06/10/2022
- Cancellation or suspensionAU D00884 (Revocation of a TGA certificate under section 41ES of the Therapeutic Goods Act 1989)Regulatory action due to Voluntary revocation at the request of the manufacturer, effective 17/03/2023
- Cancellation or suspensionAU Q00121 (Revocation of a TGA certificate under section 41ES of the Therapeutic Goods Act 1989)Regulatory action due to Voluntary revocation at the request of the manufacturer, effective 06/10/2022
- Cancellation or suspensionAU Q00133, AU D00135 (Revocation of a TGA certificate under section 41ES of the Therapeutic Goods Act 1989)Regulatory action due to Voluntary revocation at the request of the manufacturer, effective 24/03/2023
- Cancellation or suspensionAU Q00135, AU D00151, AU D00317, AU D00475 (Revocation of a TGA certificate under section 41ES of the Therapeutic Goods Act 1989)Regulatory action due to Voluntary revocation at the request of the manufacturer, effective 06/10/2022
- Cancellation or suspensionAU Q00162, AU D00165, AU D00269, AU D00276, AU D00867 (Revocation of a TGA certificate under section 41ES of the Therapeutic Goods Act 1989.)Regulatory action due to Voluntary revocation at the request of the manufacturer, effective 13/04/2023
- Cancellation or suspensionAU Q00173 (Revocation of a TGA certificate under section 41ES of the Therapeutic Goods Act 1989)Regulatory action due to Voluntary revocation at the request of the manufacturer, effective 28/02/2023
- Cancellation or suspensionAU Q00254, AU D00249, AU D00286 (Revocation of a TGA certificate under section 41ES of the Therapeutic Goods Act 1989)Regulatory action due to Voluntary revocation at the request of the manufacturer, effective 17/03/2023
- Cancellation or suspensionAU Q00365, AU D00441, AU D00711 (Revocation of a TGA certificate under section 41ES of the Therapeutic Goods Act 1989)Regulatory action due to Voluntary revocation at the request of the manufacturer, effective 07/11/2022
- Cancellation or suspensionAU Q00419, AU D00631 (Revocation of a TGA certificate under section 41ES of the Therapeutic Goods Act 1989)Regulatory action due to Voluntary revocation at the request of the manufacturer, effective 17/03/2023
- Cancellation or suspensionAU Q00462, AU D00804 (Revocation of a TGA certificate under section 41ES of the Therapeutic Goods Act 1989)Regulatory action due to Voluntary revocation at the request of the manufacturer, effective 07/11/2022
- Cancellation or suspensionConvection blood/fluid warmer high-flow (Cancelled from the ARTG under subsection 41GK of the Act)Regulatory action due to The suspension of the Device from the ARTG was not revoked before the expiry date of the suspension.
- Cancellation or suspensionConvection blood/fluid warmer high-flow (Cancelled from the ARTG under subsection 41GK of the Act)Regulatory action due to The suspension of the Device from the ARTG was not revoked before the expiry date of the suspension.
- Cancellation or suspensionRoyal Mom (Cancelled from the ARTG under 30(1C) of the Act)Regulatory action due to The sponsor failed to comply within 20 working days after a notice was given under section 31.
- Cancellation or suspensionRoyal Mom (Cancelled from the ARTG under 30(1C) of the Act)Regulatory action due to The sponsor failed to comply within 20 working days after a notice was given under section 31.
- Cancellation or suspensionLiver Slim (Cancelled from the ARTG under section 30 of the Act)Regulatory action due to The medicine is not eligible for listing (paragraph 30(1A)(a) of the Act).
- Cancellation or suspensionAMCAL DRY COUGH FORTE pholcodine 4mg/mL oral liquid bottle (Cancellation from the ARTG under s.30(2)(a) of the Act)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
- Cancellation or suspensionAMCAL DRY COUGH MIXTURE pholcodine 1 mg/mL oral liquid bottle (Cancellation from the ARTG under s.30(2)(a) of the Act)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
- Cancellation or suspensionAPOHEALTH DRY COUGH RELIEF PE & NASAL DECONGESTANT oral liquid bottle (Cancellation from the ARTG under s.30(2)(a) of the Act)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
- Cancellation or suspensionAPOHEALTH DRY TICKLY COUGH RELIEF FORTE pholcodine 4 mg/mL oral liquid bottle (Cancellation from the ARTG under s.30(2)(a) of the Act)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
- Cancellation or suspensionAPOHEALTH DRY TICKLY COUGH RELIEF pholcodine 1mg/mL oral liquid bottle (Cancellation from the ARTG under s.30(2)(a) of the Act)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
- Cancellation or suspensionAPOHEALTH DRY TICKLY COUGH RELIEF pholcodine 1mg/mL oral liquid bottle (new formulation) (Cancellation from the ARTG under s.30(2)(a) of the Act)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
- Cancellation or suspensionBENADRYL DRY, TICKLY COUGH FORTE pholcodine 4mg/mL oral liquid bottle (Cancellation from the ARTG under s.30(2)(a) of the Act)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
- Cancellation or suspensionBENADRYL DRY,TICKLY COUGH oral liquid (Cancellation from the ARTG under s.30(2)(a) of the Act)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