FDA Adverse Event Malfunction Summary report: N

DASH 4000

MDR report key: 1082176 · Received July 22, 2008

Report

Report Number
1082176
Event Type
Malfunction
Date Received
July 22, 2008
Date of Event
July 14, 2008
Report Date
July 22, 2008
Manufacturer
GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES
Product Code
MHX
Product Problem
Yes
Report Source
User Facility report
Reporter Location
MA, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

ENTIRE ROOM OF DASH 4000 MONITORS SIMULTANEOUSLY ALARMED NIBP FAILURE. ALL PATIENTS CHECKED AND WERE FINE. MONITORS WERE ALL RESET AND PROBLEM DID NOT RECUR. I WAS TOLD THAT THE MONITORS IN OUR NEWLY OPENED CARDIOVASCULAR CENTER ALARMED THE SAME FAILURE AT THE SAME TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 DASH 4000 MONITOR, PHYSIOLOGICAL MHX GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES DASH 4000 *

Patients

Seq Age Sex Outcome Treatment
1 *