FDA Adverse Event Malfunction Summary report: N

ORTHO SUMMIT SAMPLE HANDLING SYSTEM

MDR report key: 1000896 · Received January 22, 2008

Report

Report Number
2250051-2008-80049
Event Type
Malfunction
Date Received
January 22, 2008
Date of Event
August 12, 2007
Report Date
January 21, 2008
Manufacturer
HAMILTON BONADUZ, AG
Product Code
JTC
Product Problem
Yes
Report Source
Distributor report
Reporter Location
AZ, US
Reporter Occupation
MEDICAL TECHNOLOGIST

Narratives

Description of Event or Problem · 1

THE BARCODE SCANNER ON THE ORTHO SUMMIT HANDLING SYS INSTRUMENT MISREAD SAMPLE BARCODE. A BARCODE MISREAD COULD RESULT IN A SAMPLE FROM ONE PT BEING MISINTERPRETED FOR ANOTHER. NO DEATH OR SERIOUS INJURY WAS ASSOCIATED WITH THIS INCIDENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ORTHO SUMMIT SAMPLE HANDLING SYSTEM SAMPLE PIPETTER JTC HAMILTON BONADUZ, AG 7003009 *

Patients

Seq Age Sex Outcome Treatment
1 *