FDA Adverse Event Malfunction Summary report: N

CARESCAPE

MDR report key: 1061343 · Received June 9, 2008

Report

Report Number
1061343
Event Type
Malfunction
Date Received
June 9, 2008
Date of Event
May 9, 2008
Report Date
June 9, 2008
Manufacturer
GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES
Product Code
MHX
Product Problem
Yes
Report Source
User Facility report
Reporter Location
MA, US

Narratives

Description of Event or Problem · 1

ANESTHESIOLOGIST OBSERVED A SERIES OF UNLIKELY NBP READINGS, "PUMP TIMEOUT"/ "NO DETERMINATION" MESSAGES, BEFORE THE "NBP HARDWARE MALFUNCTION" MESSAGE APPEARED.====================== MANUFACTURER RESPONSE FOR MULTI-PARAMETER MODULE, PATIENT DATA MODULE======================GE WILL HELP US TO INSTALL NEW POINT RELEASE SOFTWARE TO FIX THE "NBP HARDWARE MALFUNCTION" ALARM.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CARESCAPE MONITOR, MULTI-PARAMETER MODULE MHX GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES * *

Patients

Seq Age Sex Outcome Treatment
1 *