The COVID-19 pandemic post-market review of facemasks is now closed.
Non-compliant facemasks are subject to recall action consistent with our standard, non-pandemic approach.
To keep everyone informed about our post-market review of face masks, we are publishing information about masks that require amendments to comply with Australian regulatory labelling requirements, or require their ARTG entry to be amended.
Examples of non-compliances include:
- Australian sponsor information and address are missing in the labelling;
- Manufacturer's details are incomplete or absent;
- Some product identifying information, including information about the product is not available or provided in a language other than English;
- Information relating to the product claims or compliance to standards is incomplete, inaccurate, or provided in a language other than English;
- Incorrect Global Medical Device Nomenclature (GMDN) code was chosen; or
- Intended purpose of the device was found to contain incorrect or misleading information.
Further information on interpreting face mask labelling claims is available on the TGA website.
Given the demand for face masks during the COVID-19 pandemic, the TGA may consent to the import, supply, or export of face masks that do not currently meet the labelling requirements of Essential Principle 13 for a limited period of time.
Where non-compliance is identified, sponsors can submit an application to the TGA seeking our consent to import, supply or export a medical device that does not comply with the Essential Principles. Each application is assessed with consideration to the relative risk related to the non-compliance, and the mitigations that the manufacturer or sponsor has put in place. Sponsors have continued responsibility to demonstrate the safety and performance of any medical device supplied.
ARTG entry variations
Where inaccuracies have been noted with information the sponsor has provided for an ARTG entry, the TGA will work with the sponsor to rectify the issue. These variations can also be initiated by the sponsor. Variations are recorded here for transparency to users. Further information, and the request form, for variation of ARTG entries under section 9D of the Therapeutic Goods Act 1989.
For more information about face masks visit Face masks and COVID-19.
When the TGA has processed and accepted these applications, they will appear in Non compliance notices. Click the button below to view them.