Report an adverse event

Adverse Events (AEs) in relation to medical devices in the UK should be reported through the Medicines and Healthcare Products Regulatory Agency (MHRA) Yellow Card Scheme.

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Residents of the United Kingdom

Reporting forms and information can be found at https://yellowcard.mhra.gov.uk/.

Members of the public (patients) can report Adverse Events (AEs) through the Yellow Card Scheme as well, so don’t need to consult a doctor first.

Residents of Ireland

If you are a resident of Ireland, Adverse Events should be reported to the Health Products Regulatory Authority (HPRA) by visiting www.hpra.ie.

You can also choose to report a suspected adverse event to us by using our contact form.