Product Complaint and Adverse Event Reporting Statement

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 on +44 (0)1604 704603, 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 to the MHRA.
Reporting forms and information can be found at:
www.mhra.gov.uk/safetyinformation/reportingsafetyproblems/index.htm