MalfunctionHCG
Device, Neurovascular Embolization
Received Jun 22, 2026 · Event occurred May 16, 2026
Report 3008881809-2026-00380 · MDR key 25587129
Device
Generic name
Device, Neurovascular Embolization
Manufacturer
Stryker Neurovascular CorkProduct problems
- Premature Separation
Patient
Unknown
- No Clinical Signs, Symptoms or Conditions
Narrative
Description of Event or Problem
IT WAS REPORTED DURING PROCEDURE, THE SUBJECT COIL WAS DETACHED UNINTENTIONALLY. THE PHYSICIAN PUSHED THE DETACHED COIL (SUBJECT DEVICE) WITH THE PUSHER WIRE INTO THE ANEURYSM. THERE WERE NO ISSUES AFTERWARDS. NO CLINICAL CONSEQUENCES WERE REPORTED TO THE PATIENT DUE TO THIS EVENT.