inforMED
InjuryQKA

ITIND, WITH SNARE, STERILE

Received May 22, 2026 · Event occurred Apr 27, 2026

Report 2429304-2026-00058 · MDR key 25255745

Device

Generic name

Wa2ita00

Manufacturer

Medi-tate Ltd.

Model number

WA2ITA00

Lot number

UISI3022024-2

Product problems

  • Adverse Event Without Identified Device or Use Problem

Patient

NA · Unknown

  • Urinary Retention

Narrative

Description of Event or Problem

IT WAS REPORTED THAT THE PATIENT WAS UNABLE TO URINATE SINCE THE ITIND PROCEDURE. THE PATIENT PRESENTED TO THE EMERGENCY ROOM AROUND MIDNIGHT WITH ACUTE URINARY RETENTION. IT WAS NOTED THAT THE BLADDER SCAN SHOWED OVER 800 ML OF FLUIDS AND A CATHETER WAS PLACED TO DRAIN THE BLADDER. THE PATIENT WAS THEN DISCHARGE WITH A CATHETER AND URINE BAG IN PLACED. THE PLAN IS TO KEEP THE CATHETER UNTIL THE RETRIEVAL OF THE ITIND DEVICE. THERE WERE NO FURTHER REPORTS OF PATIENT HARM.