FDA Adverse Event Malfunction Summary report: N

ORTHO SUMMIT SAMPLE HANDLING SYSTEM

MDR report key: 278716 · Received May 16, 2000

Report

Report Number
2250051-2000-00156
Event Type
Malfunction
Date Received
May 16, 2000
Date of Event
April 11, 2000
Report Date
April 12, 2000
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 WHILE RUNNING AN ANTIBODY SCREENING ASSAY, SUMMIT SAMPLE HANDLER DID NOT PIPETTE SAMPLE IN WELLS B5, C5, D5, E5, F5 AND G5 AND DID NOT GIVE AN ERROR MESSAGE. AN ORTHO FIELD SERVICE ENGINEER WAS DISPATCHED AND FOUND THAT THE TIP CLAMP SLEEVE WAS STUCK TO THE TIP CLAMP IN POSITION 5. THE TIP CLAMP WAS REPLACED. NO DEATH OR SERIOUS INJURY WAS ASSOCIATED WITH THIS EVENT. THIS REPORT CORRESPONDS TO ORTHO-CLINICAL DIAGNOSTICS COMPLAINT NUMBER 00-01698-04.

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