FDA Adverse Event Death Summary report: N

MERGE CARDIO

MDR report key: 21656629 · Received March 20, 2025

Report

Report Number
2183926-2025-00014
Event Type
Death
Date Received
March 20, 2025
Date of Event
February 8, 2025
Report Date
March 20, 2025
Manufacturer
MERGE HEALTHCARE
Product Code
LLZ
UDI-DI
00842000100928
PMA / PMN Number
K192276
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
501

Narratives

Description of Event or Problem · 0

MERGE CARDIO IS A SYSTEM INTENDED TO BE USED TO ACQUIRE, STORE, PRINT, TRANSFER, AND ARCHIVE CLINICAL INFORMATION FROM MERGE HEALTHCARE AND OTHER VENDORS SYSTEMS INCLUDING IMAGES, HEMODYNAMIC STUDIES AND REPORTS, MEASUREMENTS (VIA IMPORT FROM DICOM STRUCTURED REPORTING, TEXT FILES OR OPTICAL CHARACTER RECOGNITION OF MEASUREMENTS CAPTURED ON IMAGES) AND CARDIOLOGY SIGNAL (WAVEFORM) DATA. MERGE CARDIO IS INTENDED TO ALLOW USERS TO REVIEW DIAGNOSTIC AND NON-DIAGNOSTIC QUALITY IMAGES, ANNOTATE STUDIES, PERFORM DIGITAL SUBTRACTION ON IMAGES, TO PERFORM QUANTITATIVE MEASUREMENTS ON IMAGES (INCLUDING BUT NOT LIMITED TO QUANTITATIVE CORONARY ANALYSIS, LEFT VENTRICULAR ANALYSIS, TIME, AREA, LENGTH, VELOCITY, ANGLE, VOLUME, AND VELOCITY-TIME INTEGRALS), TO GENERATE PHYSICIAN GENERATED CLINICAL REPORTS (VIA STRUCTURE REPORTING AND TEMPLATE BASED TOOLS), AND TO STORE THIS INFORMATION IN A DATABASE. ON 02/19/2025, A CUSTOMER CONTACTED MERGE HEALTHCARE FOR ASSISTANCE WITH MERGE CARDIO'S STUDY LIST FILTERS. MERGE TECHNICAL SUPPORT REMOTELY CONNECTED TO THE CUSTOMER'S SYSTEM TO ASSIST WITH FILTER QUESTIONS. THE CUSTOMER WAS ATTEMPTING TO LOCATE A ECHOCARDIOGRAM PATIENT STUDY PERFORMED ON (B)(6) 2025 AND WAS UNABLE TO CREATE A NEW FILTER TO LOCATE THE IMAGING STUDY. TECHNICAL SUPPORT PROVIDED ASSISTANCE TO ENABLE THE CUSTOMER TO CREATE THE STUDY LIST FILTER. MERGE TECHNICAL SUPPORT ASSISTED THE CUSTOMER WITH FINDING THE STUDY AND CONFIRMED THAT THE NEW STUDY LIST FILTER WORKED AS EXPECTED. THE CUSTOMER REPRESENTATIVE MENTIONED TO TECHNICAL SUPPORT THAT THE PATIENT HAD PASSED AWAY ON (B)(6) 2025. MERGE HEALTHCARE FOLLOWED UP WITH THE CUSTOMER TO GATHER MORE INFORMATION AND DETERMINED THAT THE PATIENT OUTCOME WAS DUE TO A PREEXISTING CONDITION. BASED ON THE AVAILABLE INFORMATION, MERGE CARDIO IS PERFORMING AS DESIGNED AND DID NOT CAUSE OR CONTRIBUTE TO THE PATIENT OUTCOME. IF NEW INFORMATION BECOMES AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
508574 MERGE CARDIO SYSTEM, IMAGE PROCESSING, RADIOLOGICAL LLZ MERGE HEALTHCARE 12.1 00842000100928

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Death