FDA Adverse Event Malfunction Summary report: N

MICROLAB AT PLUS 2

MDR report key: 456868 · Received April 24, 2003

Report

Report Number
2915796-2003-00012
Event Type
Malfunction
Date Received
April 24, 2003
Date of Event
March 18, 2003
Report Date
April 24, 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 IN MARCH 2003 OF AN EVENT THAT OCCURRED IN 2003, IN WHICH THE HAMILTON MICROLAB AT +2 INSTRUMENT REPORTEDLY DID NOT PIPETTE SAMPLE INTO WELL C9 AND DID NOT GENERATE AN ERROR MESSAGE. 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