Vigilance & Safety
Report a device issue or adverse event
Patient safety is our first responsibility. If you have experienced or witnessed a problem with one of our devices, please tell us - every report is logged and investigated.
Post-market surveillance
Every report matters
Complaints and adverse-event reports feed directly into our quality management system and, where required, are escalated to the relevant regulatory authorities.
Medical emergency?
If a patient is in immediate danger, contact your local emergency services first. This form is for reporting device-related issues, not for emergency clinical support.
- Reports may be submitted by clinicians, patients, carers, distributors or any member of the public.
- You can also reach our quality team directly at contact@sardharamedical.com.