FDA Adverse Event Malfunction Summary report: N

CCU,MODULAR,IMAGE1 S X-LINK,US

MDR report key: 22472954 · Received July 10, 2025

Report

Report Number
2027009-2025-01192
Event Type
Malfunction
Date Received
July 10, 2025
Date of Event
June 11, 2025
Report Date
July 25, 2025
Manufacturer
KARL STORZ IMAGING
Product Code
FET
UDI-DI
04048551356562
PMA / PMN Number
K160044
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

THE DEVICE IN QUESTION WAS RETURNED MANUFACTURER. THIS INFORMATION IS REFLECTED IN SECTION D9. THE EVALUATION IS ANTICIPATED, BUT NOT YET BEGUN. THE INVESTIGATION WILL BE PERFORMED BY A DESIGNATED KARL STORZ EMPLOYEE. THE EVENT IS FILED UNDER INTERNAL KARL STORZ COMPLAINT ID: (B)(4).

Additional Manufacturer Narrative · 0

DEVICE EVALUATION: COMPLAINT VERIFIED - INTERMITTENT IMAGE DROP. A FUNCTIONAL TEST CONFIRMED THE CUSTOMER'S COMPLAINT. MANIPULATING THE IML CONNECTOR COULD INDUCE THE INTERMITTENT IMAGE DROP FAILURE. A VISUAL INSPECTION WAS UNABLE TO IDENTIFY ANY OBVIOUS ISSUES WITH THE IML CONNECTOR. CLEANING THE CONNECTOR DID NOT RESOLVE THE ISSUE. THE ISSUE OCCURRED WITH MULTIPLE IML TEST FIXTURE CABLES, INDICATING THE ISSUE RESIDES WITH THE MOTHERBOARD CONNECTION. THE IML CONNECTOR CAN'T BE REPLACED AT KARL STORZ - GOLETA, SO A MOTHERBOARD REPLACEMENT WILL BE REQUIRED. THE CCU IS OVER 6 YEARS OLD, AND THE CONNECTOR HAS BECOME INTERMITTENT DUE TO NORMAL WEAR AND TEAR. THE EVENT IS FILED UNDER INTERNAL KARL STORZ COMPLAINT ID: (B)(4).

Description of Event or Problem · 0

ACCORDING TO THE INFORMATION RECEIVED, THE DEVICE GIVING ISSUES WITH IMAGE OUTPUT EXPERIENCING STATICY IMAGE AND SOMETIMES GOES BLANK. NO DEATH OR (UNANTICIPATED) SERIOUS DETERIORATION IN STATE OF HEALTH REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1119514 CCU,MODULAR,IMAGE1 S X-LINK,US CCU,MODULAR,IMAGE1 S X-LINK,US FET KARL STORZ IMAGING TC301US 04048551356562

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown