FDA Adverse Event Malfunction Summary report: N

MICROLAB AT PLUS 2

MDR report key: 436436 · Received January 3, 2003

Report

Report Number
2915796-2003-00002
Event Type
Malfunction
Date Received
January 3, 2003
Date of Event
December 3, 2002
Report Date
January 2, 2003
Manufacturer
HAMILTON BONADUZ AG
Product Code
JTC
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TN, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

HAMILTON CO WAS INFORMED OF AN EVENT THAT OCCURRED IN 2002, IN WHICH THE HAMILTON MICROLAB AT +2 INSTRUMENT REPORTEDLY TRANSPOSED THE LOCATIONS OF BARCODES FOR SAMPLE IDENTIFICATION. NO DEATH OR INJURY RESULTED FROM THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MICROLAB AT PLUS 2 MICROTITER DILUTING/DISPENSING JTC HAMILTON BONADUZ AG NA NA

Patients

Seq Age Sex Outcome Treatment
1 NA Other