FDA Adverse Event Malfunction Summary report: N

UROLOGY SET

MDR report key: 24686734 · Received March 25, 2026

Report

Report Number
24686734
Event Type
Malfunction
Date Received
March 25, 2026
Date of Event
October 29, 2025
Report Date
March 13, 2026
Manufacturer
THERMEDX, LLC
Product Code
HRX
Product Problem
Yes
Report Source
User Facility report
Reporter Location
WA
Reporter Occupation
003

Narratives

Description of Event or Problem · 0

THE PORT LEAKED FROM THE CARTRIDGE. SINCE IT WAS A QUICK PROCEDURE, STAFF WAS ABLE TO COMPLETE DESPITE THE LEAKAGE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
746448 UROLOGY SET ARTHROSCOPE HRX THERMEDX, LLC LL0006 115223

Patients

Seq Age Sex Outcome Treatment
1 32 YR Male