FDA Adverse Event Malfunction Summary report: N

ORTHO SUMMIT SAMPLE HANDLER

MDR report key: 177477 · Received July 13, 1998

Report

Report Number
2250051-1998-00519
Event Type
Malfunction
Date Received
July 13, 1998
Date of Event
June 22, 1998
Report Date
July 9, 1998
Manufacturer
HAMILTON BONADUZ AG
Product Code
JTC
Product Problem
Yes
Report Source
Distributor report
Reporter Location
MI, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

THE CUSTOMER REPORTED THAT DURING AN HIV P24 ANTIGEN ASSAY, THE SAMPLE BARCODES IN POSITIONS A10 AND B10 WERE BOTH MISREAD. SUMMIT SAMPLE HANDLER, WAS IN USE. NO DEATH OR SERIOUS INJURY WAS ASSOCIATED WITH THIS EVENT. AN ORTHO FIELD SERVICE ENGINEER WAS DISPATCHED. THIS REPORT CORRESPONDS TO ORTHO-CLINICAL DIAGNOSTICS, INC. COMPLAINT NUMBER 98-02799-06.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ORTHO SUMMIT SAMPLE HANDLER SAMPLE HANDLER JTC HAMILTON BONADUZ AG 135028 NA

Patients

Seq Age Sex Outcome Treatment
1 NA Other