Adverse incidents

The Medicines and Healthcare products Regulatory Agency (MHRA)* is responsible for receiving and co-ordinating adverse incident reports relating to medical devices (including breast implants). Reports may be made by device users, patients or manufacturers.

*The MHRA was formed from a merger of the Medicines Control Agency (MCA) and the Medical Devices Agency (MDA) on 1st April 2003.


Page last modified: 26 November 2007