InjuryDQY
UNKNOWN_NEUROVASCULAR_PRODUCT
Received May 26, 2026 · Event occurred May 5, 2026
Report 3008881809-2026-00337 · MDR key 25280446
Device
Product problems
- Adverse Event Without Identified Device or Use Problem
Patient
Not reported
- Aneurysm
Narrative
Description of Event or Problem
IT WAS REPORTED THAT 1 DAY POST PROCEDURE FOR AN INTRACRANIAL ANEURYSM, THE PATIENT DEVELOPED RIGHT GROIN PSEUDOANEURYSM. IT WAS TREATED WITH ULTRASOUND GUIDED THROMBIN INJECTION. THE EVENT WAS CAUSALLY RELATED TO PROCEDURE AND PROBABLY RELATED TO SUBJECT LONG SHEATH THAT WAS USED DURING THE PROCEDURE. THE EVENT WAS CONSIDERED AS A SERIOUS ADVERSE EVENT. NO FURTHER INFORMATION IS AVAILABLE.