FDA Adverse Event Malfunction Summary report: N

MCKESSON ARCHIVAL SYSTEM

MDR report key: 7784626 · Received August 15, 2018

Report

Report Number
7784626
Event Type
Malfunction
Date Received
August 15, 2018
Date of Event
January 25, 2018
Report Date
August 2, 2018
Manufacturer
MCKESSON MEDICAL IMAGING COMPANY
Product Code
LLZ
Product Problem
Yes
Report Source
User Facility report
Reporter Location
FL
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Description of Event or Problem · 1

UNABLE TO LOCATE FILMS ON MCKESSON SYSTEM. PATIENT WAS DONE IN CATHETER LAB. WORK ORDER PUT INTO IS, BUT THERE WAS AN ERROR MESSAGE ON THE COMPUTER DURING THIS TIME. THE FILMS COULD NOT BE TRANSFERRED OVER UNTIL THE ERROR MESSAGE WAS CLEARED. ONCE THE ERROR MESSAGE WAS CORRECTED, THE FILMS WERE AVAILABLE. ALL FILMS FOR THIS PATIENT ARE PRESENT. THERE IS A PROCESS IN PLACE SO THAT THIS WILL NOT HAPPEN. FILMS ARE TO BE CHECKED DAILY TO BE SURE THEY HAVE TRANSFERRED OVER TO MCKESSON. ANY MISSING FILMS DUE TO ERROR MESSAGES SHOULD BE ADDRESSED IN REAL TIME. CATH LAB ASSISTANT NURSE MANAGER HUDDLED WITH TEAM MEMBERS REGARDING THIS PROCESS AND TO BE SURE THAT THEY ARE FOLLOWING IT DAILY AND WITH ALL CASES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
628870 MCKESSON ARCHIVAL SYSTEM SYSTEM, IMAGE PROCESSING, RADIOLOGICAL LLZ MCKESSON MEDICAL IMAGING COMPANY

Patients

Seq Age Sex Outcome Treatment
1 11315 DA