Adverse Event 

Any medical device product quality complaints (including medical device adverse incidents) relating to Baxter products can be
reported directly to the Baxter Country Quality Assurance Team:

In the UK on +44 (0)1604 704603, or by email to [email protected]
n Ireland on +353 (0)1 2065500 or by email to [email protected]

Alternatively please report directly to your Baxter Representative, who will take the details and forward to the Baxter Country
Quality Assurance Team.

Medical device adverse incidents should also be reported: In the UK to the MHRA. Reporting forms and information can be found at: Report a problem with a medicine or medical device - GOV.UK (www.gov.uk)

In Ireland to the HPRA. Reporting forms and information can be found at: http://www.hpra.ie/homepage/about-us/report-an-issue