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.

Find out more about Cancellations and Suspensions.

1780 result(s) found, displaying 726 to 750

Mask, surgical, single use (Cancellation from the ARTG under subsection 41GM(1) of the Act.)

6 July 2021

Cancellation or suspension

Regulatory action due to Non response to a s41JA, effective 06/07/2021
Mask, surgical, single use (Cancellation from the ARTG under subsection 41GM(1) of the Act.)

6 July 2021

Cancellation or suspension

Regulatory action due to Non response to a s41JA, effective 06/07/2021
Mask, surgical, single use (Cancellation from the ARTG under subsection 41GM(1) of the Act.)

6 July 2021

Cancellation or suspension

Regulatory action due to Non response to a s41JA, effective 06/07/2021
Mask, surgical, single use (Cancellation from the ARTG under subsection 41GM(1) of the Act.)

6 July 2021

Cancellation or suspension

Regulatory action due to Non response to a s41JA, effective 06/07/2021
Mask, surgical, sinlge use (Cancellation from the ARTG under subsection 41GM(1) of the Act.)

6 July 2021

Cancellation or suspension

Regulatory action due to Non response to a s41JA, effective 06/07/2021
Public respirator, single-use (Cancellation from the ARTG under subsection 41GM(1) of the Act.)

6 July 2021

Cancellation or suspension

Regulatory action due to Non response to a s41JA, effective 06/07/2021
Surgical/medical respirator, single-use (Cancellation from the ARTG under subsection 41GM(1) of the Act.)

6 July 2021

Cancellation or suspension

Regulatory action due to Non response to a s41JA, effective 06/07/2021
Surgical/medical respirator, single-use (Cancellation from the ARTG under subsection 41GM(1) of the Act.)

6 July 2021

Cancellation or suspension

Regulatory action due to Non response to a s41JA, effective 06/07/2021
Mask, surgical, single use (Cancellation from the ARTG under subsection 41GM(1) of the Act.)

5 July 2021

Cancellation or suspension

Regulatory action due to Non response to a s41JA, effective 05/07/2021
Mask, surgical, single use (Cancellation from the ARTG under subsection 41GM(1) of the Act.)

5 July 2021

Cancellation or suspension

Regulatory action due to Non response to a s41JA, effective 05/07/2021
Surgical/medical respirator, single-use (Cancellation from the ARTG under subsection 41GN(1) of the Act.)

4 July 2021

Cancellation or suspension

Regulatory action due to The safety and performance of the kind of device is unacceptable, effective 04/07/2021
Mask, surgical, single use (Cancellation from the ARTG under subsection 41GM(1) of the Act.)

3 July 2021

Cancellation or suspension

Regulatory action due to Non response to a s41JA, effective 03/07/2021
Mask, surgical, single use (Cancellation from the ARTG under subsection 41GM(1) of the Act.)

2 July 2021

Cancellation or suspension

Regulatory action due to Non response to a s41JA, effective 02/07/2021
Mask, surgical, single use (Cancellation from the ARTG under subsection 41GM(1) of the Act.)

2 July 2021

Cancellation or suspension

Regulatory action due to Non response to a s41JA, effective 02/07/2021
Mask, surgical, single use (Cancellation from the ARTG under subsection 41GM(1) of the Act.)

2 July 2021

Cancellation or suspension

Regulatory action due to Non response to a s41JA, effective 02/07/2021
COVID 19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma) (Cancellation by the Secretary of the device under s41GN(1) of the Act)

30 June 2021

Cancellation or suspension

Regulatory action due to Failure to respond to Proposal to Cancel under s 41GN(2) of the Act, effective 30/06/2021
SARS-CoV-2 IgM/IgG Antibody Test Kit (s41GN(1) Cancellation of some medical devices of the kind within the ARTG)

30 June 2021

Cancellation or suspension

Regulatory action due to Failure to respond to s41GN(2) Proposal to cancel, effective 30/06/2021
Severe acute respiratory syndrome-associated coronavirus IVDs (Cancellation from the ARTG under section 41GN(1) of the Act.)

30 June 2021

Cancellation or suspension

Regulatory action due to Failure to comply with a condition of inclusion., effective 30/06/2021
Public facemask, reusable (Cancellation from the ARTG under subsection 41GN(1) of the Act.)

25 June 2021

Cancellation or suspension

Regulatory action due to Failure to comply with a condition of inclusion, effective 25/06/2021
Severe acute respiratory syndrome-associated coronavirus IVDs (Cancellation from the ARTG under subsection 41GM(1) of the Act.)

21 June 2021

Cancellation or suspension

Regulatory action due to Non response to a s41JA, effective 21/06/2021
APO-RANITIDINE ranitidine 150mg (as hydrochloride) tablet blister pack (Suspension from the ARTG under s.29D(1)(b))

17 June 2021

Cancellation or suspension

Regulatory 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 17/06/2021
APO-RANITIDNE ranitidine 300mg (as hydrochloride) tablet blister pack (Suspension from the ARTG under s.29D(1)(b))

17 June 2021

Cancellation or suspension

Regulatory 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 17/06/2021
AUSRAN ranitidine 150mg (as hydrochloride) tablet blister pack (Suspension from the ARTG under s.29D(1)(b))

17 June 2021

Cancellation or suspension

Regulatory 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 17/06/2021
AUSRAN ranitidine 150mg (as hydrochloride) tablet bottle (Suspension from the ARTG under s.29D(1)(b))

17 June 2021

Cancellation or suspension

Regulatory 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 17/06/2021
AUSRAN ranitidine 300mg (as hydrochloride) tablet blister pack (Suspension from the ARTG under s.29D(1)(b))

17 June 2021

Cancellation or suspension

Regulatory 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 17/06/2021

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Cancellations and suspensions

Filter results

Action

Date of effect

Mask, surgical, single use (Cancellation from the ARTG under subsection 41GM(1) of the Act.)

Mask, surgical, single use (Cancellation from the ARTG under subsection 41GM(1) of the Act.)

Mask, surgical, single use (Cancellation from the ARTG under subsection 41GM(1) of the Act.)

Mask, surgical, single use (Cancellation from the ARTG under subsection 41GM(1) of the Act.)

Mask, surgical, sinlge use (Cancellation from the ARTG under subsection 41GM(1) of the Act.)

Public respirator, single-use (Cancellation from the ARTG under subsection 41GM(1) of the Act.)

Surgical/medical respirator, single-use (Cancellation from the ARTG under subsection 41GM(1) of the Act.)

Surgical/medical respirator, single-use (Cancellation from the ARTG under subsection 41GM(1) of the Act.)

Mask, surgical, single use (Cancellation from the ARTG under subsection 41GM(1) of the Act.)

Mask, surgical, single use (Cancellation from the ARTG under subsection 41GM(1) of the Act.)

Surgical/medical respirator, single-use (Cancellation from the ARTG under subsection 41GN(1) of the Act.)

Mask, surgical, single use (Cancellation from the ARTG under subsection 41GM(1) of the Act.)

Mask, surgical, single use (Cancellation from the ARTG under subsection 41GM(1) of the Act.)

Mask, surgical, single use (Cancellation from the ARTG under subsection 41GM(1) of the Act.)

Mask, surgical, single use (Cancellation from the ARTG under subsection 41GM(1) of the Act.)

COVID 19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma) (Cancellation by the Secretary of the device under s41GN(1) of the Act)

SARS-CoV-2 IgM/IgG Antibody Test Kit (s41GN(1) Cancellation of some medical devices of the kind within the ARTG)

Severe acute respiratory syndrome-associated coronavirus IVDs (Cancellation from the ARTG under section 41GN(1) of the Act.)

Public facemask, reusable (Cancellation from the ARTG under subsection 41GN(1) of the Act.)

Severe acute respiratory syndrome-associated coronavirus IVDs (Cancellation from the ARTG under subsection 41GM(1) of the Act.)

APO-RANITIDINE ranitidine 150mg (as hydrochloride) tablet blister pack (Suspension from the ARTG under s.29D(1)(b))

APO-RANITIDNE ranitidine 300mg (as hydrochloride) tablet blister pack (Suspension from the ARTG under s.29D(1)(b))

AUSRAN ranitidine 150mg (as hydrochloride) tablet blister pack (Suspension from the ARTG under s.29D(1)(b))

AUSRAN ranitidine 150mg (as hydrochloride) tablet bottle (Suspension from the ARTG under s.29D(1)(b))

AUSRAN ranitidine 300mg (as hydrochloride) tablet blister pack (Suspension from the ARTG under s.29D(1)(b))

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