FDA Adverse Event Malfunction Summary report: N

HX2 TEMPERATURE MANAGEMENT SYSTEM

MDR report key: 1940681 · Received December 17, 2010

Report

Report Number
1828100-2010-02826
Event Type
Malfunction
Date Received
December 17, 2010
Date of Event
September 24, 2010
Report Date
December 17, 2010
Manufacturer
TERUMO CARDIOVASCULAR SYSTEMS CORP.
Product Code
DWC
PMA / PMN Number
K071521
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WI, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

EVAL IN PROGRESS, BUT NOT YET CONCLUDED.

Description of Event or Problem · 1

DURING ROUTINE TESTING OF THE DEVICE AT THE SERVICE CENTER, THE USER OBSERVED AN EOD ERROR CODE MESSAGE. NO OTHER DETAILS REGARDING THE NATURE OF THE EVENT WERE PROVIDED. SINCE THE EVENT OCCURRED DURING ROUTINE TESTING OF THE DEVICE, THERE WAS NO PT INVOLVEMENT DURING THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HX2 TEMPERATURE MANAGEMENT SYSTEM COOLING & HEATING SYSTEM DWC TERUMO CARDIOVASCULAR SYSTEMS CORP. 809810

Patients

Seq Age Sex Outcome Treatment
1