To report local or systemic complications occurring after implantation, please contact the appropriate agency in your country. Adverse event reporting forms for medical devices may be accessed here:
United States
Medwatch
FDA
*You may use your initials in the "Patient Identifier" box.
Australia
IRIS: Medical Device Incident Report Investigation Scheme
Therapeutic Goods Administration
New Zealand
Medsafe
Ministry of Health
Canada
Medical Device Compliance Unit
Health Canada
Medical Devices Problem Report Form
United Kingdom
Adverse Incident Centre
Medicines and Healthcare products Regulatory Agency
The information on this website is presented for educational purposes.