FDA Adverse Event Malfunction Summary report: N

SCOPEYE

MDR report key: 24883976 · Received April 14, 2026

Report

Report Number
MW5186829
Event Type
Malfunction
Date Received
April 14, 2026
Report Date
April 10, 2026
Manufacturer
MEDITHINQ CO., LTD.
Product Code
LMD
Product Problem
Yes
Report Source
Voluntary report
Reporter Occupation
UNKNOWN
Health Professional
*

Narratives

Description of Event or Problem · 0

WE HAVE RECEIVED A PRODUCT REPORT INVOLVING A NON-(B)(6) PRODUCT AND ARE SENDING YOU THE INFORMATION IN ACCORDANCE WITH 21 CFR 803.22. BELOW IS A BRIEF DESCRIPTION OF THE INFORMATION RECEIVED: (B)(6) (SPINE REP) CALLED IN TO REPORT THAT THE SYSTEM WAS UNABLE TO COMMUNICATE WITH SCOPEYE AND THROUGH THE SCOPEYE LENS, ONLY THE LOGO APPEARED. SPINE REP REPORTED HE ATTEMPTED TO REBOOT BOTH THE STEALTH, TRANSMITTER, AND HEADSET. SPINE REP REPORTED THIS IS A DEMO SYSTEM THAT WAS FUNCTIONING AS INTENDED A WEEK AGO WITH A MAZOR SYSTEM AT ANOTHER SITE. TROUBLESHOOTING: SPINE REP CONFIRMED THAT THE SCOPEYE LOGO APPEARS DURING USE AND DOES NOT GO AWAY. SPINE REP CONFIRMED THAT THE POWER WAS ON TRANSMITTER, CHECKED ALL CONNECTIONS AND CABLES, AND REPORTED THAT THE POWER BUTTON WOULD TURN FROM RED TO WHITE TO LIGHT BLUE BUT THAT THE CONNECTION SYMBOL WOULD ONLY BLINK BLUE IF PRESSED OR REBOOTED BUT NEVER DISPLAYED A SOLID BLUE LIGHT. SPINE REP REPORTED AFTER THE CONNECTION SYMBOL WAS BLINKING BLUE, THE LED WOULD TURN OFF AND NOT ILLUMINATE. SPINE REP REPORTED HE CHANGED THE DISPLAY IN STEALTHSTATION CONFIGURATION TO THE CORRECT HD DISPLAY, LOGGED OUT AND BACK IN AND ISSUE PERSISTED. TS HAD SPINE REP GO INTO STEALTH APPLICATION, SPINE REP CONFIRMED THE EXTERNAL PORT WAS TURNED ON. TS RECOMMENDED SPINE REP ATTEMPT TO PAIR THE SCOPEYE AGAIN HOWEVER, SPINE REP REPORTED THIS IS A DEMO SYSTEM AND HE DOES NOT HAVE THE MANAGER PAD TO PAIR. SPINE REP REPORTED THAT THEY HAVE NOT ATTEMPTED TO DISPLAY ON EXTERNAL MONITOR OR TRANSMIT VIDEO OUT ON THE STEALTH BEFORE. SPINE REP REPORTED HE TRIED TO CONNECT THE SCOPEYE TO THIS SYSTEM AND SYSTEM SN: (B)(6) AND ISSUE PERSISTED. THIS REPORT REFLECTS INFORMATION RECEIVED BY FDA IN THE FORM OF A NOTIFICATION PER 803.22 (B)(2).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
938047 SCOPEYE SYSTEM, DIGITAL IMAGE COMMUNICATIONS, RADIOLOGICAL LMD MEDITHINQ CO., LTD.

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown