FDA Adverse Event Malfunction Summary report: N

DUAL COOLER/HEATER

MDR report key: 2153115 · Received June 17, 2011

Report

Report Number
1828100-2011-01699
Event Type
Malfunction
Date Received
June 17, 2011
Date of Event
May 19, 2011
Report Date
June 17, 2011
Manufacturer
TERUMO CARDIOVASCULAR SYSTEMS CORP.
Product Code
DWC
PMA / PMN Number
PREAMEND
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Description of Event or Problem · 1

DURING PRIMING OF THE DEVICE FOR A CARDIOPULMONARY BYPASS PROCEDURE, THE USER WAS UNABLE TO DE-AIR THE CIRCUIT. AS A RESULT, AN ALTERNATE DEVICE WAS EMPLOYED. THE USER REPORTED THE SURGICAL PROCEDURE WAS COMPLETED SUCCESSFULLY, AND THERE WERE NO ADVERSE CONSEQUENCES TO THE PT AS A RESULT OF THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 DUAL COOLER/HEATER COOLING & HEATING SYSTEM DWC TERUMO CARDIOVASCULAR SYSTEMS CORP. 11160

Patients

Seq Age Sex Outcome Treatment
1