FDA Adverse Event Malfunction Summary report: N

ORTHO SUMMIT PROCESSOR

MDR report key: 486246 · Received September 16, 2003

Report

Report Number
2250051-2003-01162
Event Type
Malfunction
Date Received
September 16, 2003
Date of Event
September 3, 2003
Report Date
September 12, 2003
Manufacturer
ORTHO-CLINICAL DIAGNOSTICS
Product Code
JTC
Product Problem
Yes
Report Source
Distributor report
Reporter Location
MA, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

THE CUSTOMER REPORTED THAT AFTER PROCESSING AN HBSAG PLATE ON OSP THE PLATE REPORT SHOWED THAT NEGATIVE ODS WERE PRESENT THROUGHOUT ROWS D AND H. NO DEATH OR SERIOUS INJURY WAS ASSOCIATED WITH THIS INCIDENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ORTHO SUMMIT PROCESSOR SAMPLE PROCESSOR JTC ORTHO-CLINICAL DIAGNOSTICS 7003015 NA

Patients

Seq Age Sex Outcome Treatment
1 NA Other