FDA Adverse Event Malfunction Summary report: N

ORTHO SUMMIT SAMPLE HANDLING SYSTEM

MDR report key: 1252419 · Received September 25, 2008

Report

Report Number
2250051-2008-80453
Event Type
Malfunction
Date Received
September 25, 2008
Date of Event
September 17, 2008
Report Date
September 25, 2008
Manufacturer
HAMILTON BONADUZ AG
Product Code
JTC
Product Problem
Yes
Report Source
Distributor report
Reporter Location
MI, US
Reporter Occupation
MEDICAL TECHNOLOGIST

Narratives

Description of Event or Problem · 1

THE ORTHO SUMMIT SAMPLE HANDLING SYSTEM INSTRUMENT REPORTEDLY PIPETTED INSUFFICIENT SAMPLE/REAGENT AND DID NOT GENERATE AN ERROR MESSAGE. 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 7003015 *

Patients

Seq Age Sex Outcome Treatment
1 *