FDA Adverse Event Malfunction Summary report: N

MTS ID TIPMASTER PIPETTOR

MDR report key: 827109 · Received November 1, 2006

Report

Report Number
1056600-2006-00324
Event Type
Malfunction
Date Received
November 1, 2006
Date of Event
September 29, 2006
Report Date
October 31, 2006
Manufacturer
MICRO TYPING SYSTEMS, INC.
Product Code
GJG
PMA / PMN Number
BK980016
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
INVALID DATA

Narratives

Additional Manufacturer Narrative · 1

THE CUSTOMER REPORTED THAT THE MTS ID TIPMASTER PIPETTOR DID NOT DISPENSE THE PROPER AMOUNT OF FLUID. IT IS UNK WHICH TESTS WERE BEING PERFORMED AT THE TIME OF THE INCIDENT. NO DEFINITIVE ROOT CAUSE WAS DETERMINED CONCERNING THE INCORRECT DISPENSE OF THE PIPETTOR. THE CUSTOMER DETECTED THE REPORTED ISSUE (FOLLOWING LABELING RECOMMENDATIONS), AND THEN REMOVED THE PIPETTOR FROM USE PREVENTING THE REPORTING OF ERRONEOUS TEST RESULTS. THE CUSTOMER WAS ADVISED TO CONTACT THEIR OCD ACCOUNT MGR REGARDING PURCHASE OF A REPLACEMENT PIPETTOR, SINCE THE INSTRUMENT WAS OUT OF WARRANTY. LABELING CAUTIONS ON THE IMPORTANCE OF DELIVERING THE CORRECT AMOUNT OF CELLS AND PLASMA/SERUM WHEN PERFORMING THE GEL TEST METHOD. THE INSTRUMENT IS A HANDHELD PIPETTOR. THE PIPETTOR IS USED IN PREPARING A MANUAL GEL TEST. A LABORATORY TECHNICIAN CLOSELY MONITORS ALL TESTS. ALL TESTS ARE QUALITATIVE. ALTHOUGH LABORATORY PRACTICES MITIGATE THE POSSIBILITY OF ERRONEOUS PT RESULTS, IF THE ALLEGED MALFUNCTION WERE TO RECUR UNDETECTED, IT COULD LEAD TO ERRONEOUS TEST RESULTS. THEREFORE, INCIDENT IS REPORTABLE.

Description of Event or Problem · 1

THE CUSTOMER REPORTED THAT THE MTS-ID TIPMASTER PIPETTOR WAS NOT DISPENSING THE CORRECT AMOUNT OF VOLUME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MTS ID TIPMASTER PIPETTOR MANUAL PIPETTOR GJG MICRO TYPING SYSTEMS, INC. MTS9640 *

Patients

Seq Age Sex Outcome Treatment
1 *