FDA Adverse Event Malfunction Summary report: N

ORTHO SUMMIT SAMPLE HANDLING SYSTEM

MDR report key: 181798 · Received August 7, 1998

Report

Report Number
2250051-1998-00535
Event Type
Malfunction
Date Received
August 7, 1998
Date of Event
July 14, 1998
Report Date
August 6, 1998
Manufacturer
HAMILTON BONADUZ AG
Product Code
JTC
Product Problem
Yes
Report Source
Distributor report
Reporter Location
FL, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

THE CUSTOMER REPORTED THAT WHILE RUNNING AN HTLV I/II ASSAY, SUMMIT SAMPLE HANDLER DID NOT PIPETTE REAGENT IN ROW 7 AND DID NOT GIVE AN ERROR MESSAGE. AN ORTHO FIELD SERVICE ENGINEER WAS DISPATCHED. NO DEATH OR SERIOUS INJURY WAS ASSOCIATED WITH THIS EVENT. THIS REPORT CORRESPONDS TO ORTHO-CLINICAL DIAGNOSTICS, INC COMPLAINT NUMBER 98-03187-07.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1 NA Other