Guidance

Reporting adverse incidents: joint replacement implants

For manufacturers reporting adverse incidents with joint replacement implants under the vigilance system.

Documents

Adverse incidents with joint replacement implants

Request an accessible format.
If you use assistive technology (such as a screen reader) and need a version of this document in a more accessible format, please email webupdates@mhra.gov.uk. Please tell us what format you need. It will help us if you say what assistive technology you use.

Details

Guidance on how to report adverse incidents with joint replacement implants. To be read in conjunction with the guidelines on a medical devices vigilance system MEDDEV 2.12/1 which sets out the general adverse incident reporting obligations on all manufacturers of medical devices including joint replacement implants.

Updates to this page

Published 1 June 2008
Last updated 30 December 2020 + show all updates
  1. This page has been updated due to the end of the transition period.

  2. First published.

Sign up for emails or print this page